Inactive / Discontinued
Substance Identification & Data
This profile provides standardized clinical and technical data for Oleth-3 Phosphate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 8Q0Z18J1VL.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 45306-73-8 and the RxNorm Concept ID (RxCUI) 1314374. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
OLETH-3 PHOSPHATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
8Q0Z18J1VL
The specific atomic composition represented as a molecular structure string.
InChIKey
C24H49O7P International Chemical Identifier digital signature for unique molecular identification.
SMILES String
PWQNOLAKMCLNJI-KTKRTIGZSA-N Line notation for describing the chemical structure and connectivity of atoms.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
C(OCCOCCOCCOP(O)(O)=O)CCCCCCC/C=C\CCCCCCCC
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Oleth-3 Phosphate. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
FDA Official Name
OLETH-3 PHOSPHATE
OF
Common Names & Synonyms
ETHANOL, 2-(2-(2-((9Z)-9-OCTADECEN-1-YLOXY)ETHOXY)ETHOXY)-, 1-(DIHYDROGEN PHOSPHATE)
CN
OLETH-3 PHOSPHATE [VANDF]
CN
OLETH-3-PHOSPHATE
CN
PEG-3 OLEYL ETHER PHOSPHATE
CN
Brand / Trade Names
CRODAFOS O3A
BN
NDC Products Containing OLETH-3 PHOSPHATE
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
Manufacturer Quick Index
Found 100 manufactured products
Adventure Ready Brands
NDC Product
After Bite Kids NDC 90107-1280
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
NDC Product
The Itch Eraser Sensitive NDC 90107-2420
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Inactive / Discontinued
Allergan, Inc.
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide And Octinoxate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
CP Skin Health Group, Inc
NDC Product
Human Otc DrugEltamd Uv Physical Rosy Tint Spf40 NDC 72043-2257
- Generic Name
- Titanium Dioxide, Zinc Oxide Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Clear Blemish-prone And Oil Balancing NDC 72043-2518
- Generic Name
- Octinoxate And Zinc Oxide Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Physical Spf41 NDC 72043-2588
- Generic Name
- Zinc Oxide And Titanium Dioxide Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Daily NDC 72043-6804
- Generic Name
- Octinoxate, Zinc Oxide Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Daily Tinted NDC 72043-6806
- Generic Name
- Octinoxate, Zinc Oxide Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Spf35 NDC 72043-6808
- Generic Name
- Octinoxate, Zinc Oxide Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
CP Skin Health Group, Inc.
NDC Product
Human Otc DrugWeightless Protection Spf 45 NDC 68726-262
- Generic Name
- Sunscreen Broad Spectrum
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugUv Skin Recovery Spf 50 NDC 72043-0333
- Generic Name
- Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugUv Skin Recovery Spf 50 Red Correcting NDC 72043-0334
- Generic Name
- Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Daily Tinted Spf40 NDC 72043-2269
- Generic Name
- Zinc Oxide And Octinoxate Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
NDC Product
Human Otc DrugEltamd Uv Shield Spf45 NDC 72043-2282
- Generic Name
- Zinc Oxide And Octinoxate Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
NDC Product
Human Otc DrugEltamd Uv Facial Spf30 Plus NDC 72043-2283
- Generic Name
- Zinc Oxide And Octinoxate Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Spf 30 Plus NDC 72043-2286
- Generic Name
- Zinc Oxide And Octinoxate Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
NDC Product
Human Otc DrugEltamd Uv Daily Spf40 NDC 72043-2289
- Generic Name
- Zinc Oxide And Octinoxate Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
NDC Product
Human Otc DrugEltamd Uv Clear Spf46 NDC 72043-2500
- Generic Name
- Zinc Oxide And Octinoxate Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Clear Tinted Spf46 NDC 72043-2520
- Generic Name
- Zinc Oxide And Octinoxate Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugUv Clear Deep Tint NDC 72043-2530
- Generic Name
- Octinoxate, Zinc Oxide Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Physical Spf41 NDC 72043-2578
- Generic Name
- Zinc Oxide And Titanium Dioxide Sunscrreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
NDC Product
Human Otc DrugUv Daily Deep Tint NDC 72043-2920
- Generic Name
- Octinoxate, Zinc Oxide Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEltamd Uv Daily Hydration NDC 72043-6813
- Generic Name
- Octisalate, Zinc Oxide Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Chattem, Inc.
NDC Product
Human Otc DrugIcy Hot Pain Relieving Cream NDC 41167-0088
- Generic Name
- Menthol And Methyl Salicylate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugArthritis Hot NDC 41167-0600
- Generic Name
- Menthol And Methyl Salicylate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Arthritis Hot NDC 41167-0600
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
Dolgencorp Inc
NDC Product
Cool Heat NDC 55910-405
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
Drmtlgy, LLC
NDC Product
Human Otc DrugBroad Spectrum Spf45 NDC 83286-008
- Generic Name
- Zinc Oxide, Octinoxate
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
NDC Product
Human Otc DrugTinted Moisturizer Spf 46 Universal Tint NDC 83286-009
- Generic Name
- Zinc Oxide, Octinoxate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBroad Spectrum Spf45 NDC 83286-014
- Generic Name
- Zinc Oxide, Octinoxate
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMatte Universal Tinted Moisturizer Spf46 NDC 83286-015
- Generic Name
- Zinc Oxide, Octinoxate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Genomma Lab USA Inc.
NDC Product
Ray Dol NDC 50066-057
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
Goodier Cosmetics
NDC Product
Daily Spf 20 Oleander Face Cream NDC 10477-0063
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
Goodier Cosmetics LLC
NDC Product
Zinc Oxide NDC 10477-1384
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
Haleon US Holdings LLC
NDC Product
Human Otc DrugAdvil Targeted Relief NDC 0573-6555
- Generic Name
- Camphor, Capsaicin, Menthol, Methyl Salicylate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hayden Caleel LLC
NDC Product
Human Otc DrugGlo Skin Beauty Oil Free Spf 40 NDC 60541-1000
- Generic Name
- Glo Skin Beauty Oil Free Spf 40
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kandenwood LLC
NDC Product
Level Select Menthol Camphor Roll On NDC 83191-003
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
Meijer Distribution, Inc
NDC Product
Human Otc Drug- Generic Name
- Menthol, Unspecified Form And Methyl Salicylate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Meijer, Inc.
NDC Product
Human Otc DrugBeauty Hydrating NDC 79481-0000
- Generic Name
- Homosalate, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Noxell Corporation
NDC Product
Human Otc Drug- Generic Name
- Octinoxate And Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NuCare Pharmaceuticals, Inc.
NDC Product
Human Otc DrugRugby Muscle Rub Cream NDC 68071-3789
- Generic Name
- Muscle Rub Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Human Otc DrugDr Sheffield Muscle Rub Cream NDC 68071-1624
- Generic Name
- Muscle Rub Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Dr Sheffield Muscle Rub Cream NDC 68071-2477
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
Nuvothera, Inc.
NDC Product
Human Otc DrugProsoria Psoriasis Treatment NDC 71573-102
- Generic Name
- Salicylic Acid
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugProsoria Scalp NDC 71573-116
- Generic Name
- Salicylic Acid
- Dosage Form
- Lotion/shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Prosoria Psoriasis Treatment NDC 71573-117
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Inactive / Discontinued
Patterson Dental Supply Inc
NDC Product
Topical 60 Sec Sodium Fluoride Strawberry NDC 50227-0501
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product
Topical 60 Sec Sodium Fluoride Mint NDC 50227-0511
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product
Topical 60 Sec Sodium Fluoride Bubble Gum NDC 50227-0521
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product
Topical 60 Sec Sodium Fluoride Grape NDC 50227-0531
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product
Topical 60 Sec Sodium Fluoride Orange Cream NDC 50227-0541
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Inactive / Discontinued
Person and Covey
NDC Product
Human Otc DrugSolbar Sunscreen 40 Shield NDC 0096-0692
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Peter Thomas Roth Labs, LLC
NDC Product
Human Otc DrugMax Mineral NDC 54031-020
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Philosophy, Inc.
NDC Product
Supernatural Superbeautiful Makeup Spf 15 NDC 50184-6000
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
PhotoMedex, Inc.
NDC Product
Neova Dna Damage Control - Everyday Spf 43 NDC 62362-139
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Inactive / Discontinued
NDC Product
Neova Dna Damage Control - Everyday Spf 43 NDC 62362-139
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Inactive / Discontinued
NDC Product
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
Preferred Pharmaceuticals Inc.
NDC Product
Human Otc DrugRugby Muscle Rub Cream NDC 68788-8729
- Generic Name
- Muscle Rub Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Prime Enterprises
NDC Product
Traci Lynn Skin Iluminator Broad Spectrum Spf 50 NDC 58443-0295
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Inactive / Discontinued
NDC Product
Traci Lynn Skin Iluminator Broad Spectrum Spf 50 NDC 58443-0296
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Inactive / Discontinued
Private Label Skin Care
NDC Product
Human Otc DrugSheer Defense Tinted Spf 46 NDC 72957-002
- Generic Name
- Zinc Oxide, Octinoxate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugClear Defense Spf 45 NDC 72957-003
- Generic Name
- Zinc Oxide, Octinoxate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHydro Essence Broad Spectrum Sunscreen Spf 40 NDC 72957-008
- Generic Name
- Zinc Oxide, Octinoxate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
R & R Lotion, Inc
NDC Product
Human Otc DrugBeach Club Mineral Sunscreen NDC 59555-109
- Generic Name
- Zinc Oxide, Octinoxate, Oxybenzone, And Octisalate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugI.c. Industrial Sunscreen NDC 59555-117
- Generic Name
- Zinc Oxide, Octinoxate, Oxybenzone, And Octisalate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugRugby Muscle Rub Cream NDC 0536-1349
- Generic Name
- Muscle Rub Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
SOTAC PHARMACEUTICALS PRIVATE LIMITED
NDC Product
Cold And Heat Pain Relieving Cream NDC 72351-010
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
Sheffield Pharmaceuticals LLC
NDC Product
Human Otc DrugDr Sheffield Muscle Rub Cream NDC 11527-057
- Generic Name
- Muscle Rub Cream
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Swiss-American CDMO, LLC
NDC Product
Human Otc DrugPrivate Label Moisturizing Oil Free Paraben Free Spf43 NDC 60232-0007
- Generic Name
- Sunscreen
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPrivate Label Super Light Oil-free Spf45 NDC 60232-0008
- Generic Name
- 2.75% Octinsalate, 7.50% Octinoxate, 8.00% Zinc Oxide Sunscr...
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
TAYLOR JAMES, LTD.
NDC Product
Advanced Anti-aging Eye Broad Spectrum Spf 37 Supergoop NDC 75936-120
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Inactive / Discontinued
NDC Product
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Inactive / Discontinued
Tender Corporation d/b/a Adventure Ready Brands
NDC Product
Human Otc DrugAfter Bite Kids NDC 44224-1117
- Generic Name
- Sodium Bicarbonate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugItch Eraser Sensitive NDC 44224-2421
- Generic Name
- Sodium Bicarbonate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
The Procter & Gamble Manufacturing Company
NDC Product
Human Otc Drug- Generic Name
- Octinoxate And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Octisalate, Octocrylene, And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product
Human Otc Drug- Generic Name
- Octinoxate And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Octisalate, Octocrylene, And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOlay Age Defying Classic Broad Spectrum Spf 15 NDC 84126-231
- Generic Name
- Octinoxate And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
The Tetra Corporation
NDC Product
Human Otc DrugRapid Microgel NDC 49406-005
- Generic Name
- Tolnaftate
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFormula 7 - The Solution NDC 49406-007
- Generic Name
- Tolnaftate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Formula 7 Thegel NDC 49406-008
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
Therapon Skin Health, LP
NDC Product
Theradermspf 43 Spf 43 NDC 66428-002
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Inactive / Discontinued
Topco Associates LLC
NDC Product
Loratadine NDC 36800-513
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Inactive / Discontinued
NDC Product
Human Otc DrugBeauty Hydrating NDC 36800-513
- Generic Name
- Homosalate, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Topiderm, Inc.
NDC Product
Human Otc DrugClarity Rx Physical Skin Defense Spf 50 NDC 51326-035
- Generic Name
- Zinc Oxide And Titanium Dioxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEssential Moisturizing Sunscreen NDC 51326-122
- Generic Name
- Zinc Oxide, Octinoxate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTinted Mineral Sunscreen Spf 50 NDC 51326-123
- Generic Name
- Zinc Oxide And Titanium Dioxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEssential Sheer Spf 50 NDC 51326-200
- Generic Name
- Zinc Oxide Titanium Dioxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugReplenix Tinted Sunscreen Spf 50 NDC 51326-201
- Generic Name
- Zinc Oxide And Octinoxate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugReplenix Sunscreen Spf 50 NDC 51326-220
- Generic Name
- Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
UNITED EXCHANGE CORP
NDC Product
Family Care Muscle Rub Pain Reliever NDC 65923-498
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
Velocity Pharma LLC
NDC Product
Cold And Heat Pain Relieving Cream NDC 76168-402
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
WALGREEN COMPANY
NDC Product
Walgreens Cool And Heat Muscle And Joint Relief NDC 0363-0147
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
Walmart Inc.
NDC Product
Human Otc DrugSpf Beauty NDC 79903-058
- Generic Name
- Spf Beauty
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAll Day Moisture NDC 79903-313
- Generic Name
- Homosalate, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Yoderm, Inc.
NDC Product
Apostrophe Screen Spf43 NDC 81780-007
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Inactive / Discontinued
