HYDROGENATED PALM OIL
UNII 257THB963H

Substance Identification & Data

This profile provides standardized clinical and technical data for Hydrogenated Palm Oil, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 257THB963H.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 68514-74-9 and the RxNorm Concept ID (RxCUI) 1307676. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
257THB963H
CAS Registry Number
68514-74-9
RxNorm Concept ID
1307676

Detailed Substance Profile

Preferred Name
HYDROGENATED PALM OIL
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
257THB963H
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C85243
National Cancer Institute reference terminology for clinical and research data.
Substance Type
structurallyDiverse
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
ITIS TSN
506719
Taxonomic Serial Number for species identified in the Integrated Taxonomic Information System.
NCBI Taxonomy
51953
Unique numeric identifier used to specify biological species in the NCBI database.
USDA PLANTS ID
ELGU
Botanical identifier maintained by the U.S. Department of Agriculture.
GRIN Nomen ID
14936
Identifier from the Germplasm Resources Information Network botanical database.
MPNS Record
WCS-66337
Record ID from the Kew Royal Botanic Gardens Medicinal Plants Name Service.

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Hydrogenated Palm Oil. 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

HYDROGENATED PALM OIL

Common Names & Synonyms

HYDROGENATED PALM OIL [II]
HYDROGENATED PALM OIL [NF]
OILS, PALM, HYDROGENATED
PALM OIL, HYDROGENATED

NDC Products Containing HYDROGENATED PALM OIL

This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:

Manufacturer Quick Index

→ ALIX AVIEN KOZMETIK SANAYI TICARET ANONIM SIRKETI 1
→ Allergan, Inc. 2
→ Allure Labs 1
→ Allure Labs Inc 1
→ Anna Lotan Ltd 1
→ Apcco Labs, Inc 3
→ BOTANICAL SCIENCE, INC. 1
→ Bogey Blocker LLC 1
→ Catherine Hinds Company, Inc. 1
→ Columbia Laboratories 2
→ Crown Laboratories 3
→ Cyberderm Laboratories inc. 3
→ Guthy-Renker LLC 1
→ KAVI Skin Solutions, Inc. 2
→ Marlex Pharmaceuticals, Inc. 1
→ Meaningful Beauty, LLC 2
→ Neilmed Pharmaceuticals Inc. 1
→ Patrin Pharma Inc. 2
→ Rebel Distributors Corp 1
→ Ripar Cosmetici srl 32
→ SHISEIDO AMERICAS CORPORATION 1
→ Salix Pharmaceuticals, Inc 2
→ Sandoz Inc 2
→ Unconditional Love d/b/a Hello Bello 1

ALIX AVIEN KOZMETIK SANAYI TICARET ANONIM SIRKETI

NDC Product

Alix Avien Vegan Cc Cream
NDC 82668-100

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH FINAL
Inactive / Discontinued

Allergan, Inc.

NDC Product
Human Prescription Drug

Crinone
NDC 0023-6150

Generic Name
Progesterone
Dosage Form
Gel
Route
Vaginal
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Crinone
NDC 0023-6151

Generic Name
Progesterone
Dosage Form
Gel
Route
Vaginal
Marketing
NDA
Active Listing

Allure Labs

Allure Labs Inc

NDC Product
Human Otc Drug

Spf Elio Drops 30 Glow
NDC 62742-4233

Generic Name
Zinc Oxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Anna Lotan Ltd

Apcco Labs, Inc

NDC Product
Human Otc Drug

Sunshine Hemorrhoidrelief
NDC 82126-001

Generic Name
Hemorrhoid Suppository
Dosage Form
Suppository
Route
Rectal
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Sunshine Menopauserelief
NDC 82126-002

Generic Name
Menopause Suppository
Dosage Form
Suppository
Route
Vaginal
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Sunshine Yeastrelief
NDC 82126-003

Generic Name
Vaginal Yeast Relief
Dosage Form
Suppository
Route
Rectal
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

BOTANICAL SCIENCE, INC.

NDC Product
Human Otc Drug

Advanced Protection Sunscreen Spf-30
NDC 70712-103

Generic Name
Octinoxate, Octisalate, Zinc Oxide
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Bogey Blocker LLC

NDC Product

Bogey Blocker Spf 30
NDC 83386-101

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH FINAL
Inactive / Discontinued

Catherine Hinds Company, Inc.

Columbia Laboratories

NDC Product

Prochieve
NDC 55056-0406

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Inactive / Discontinued
NDC Product

Prochieve
NDC 55056-1601

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Inactive / Discontinued

Crown Laboratories

NDC Product
Human Otc Drug

Blue Lizard Sheer Spf 50 Sunscreen
NDC 0316-2064

Generic Name
Titanium Dioxide, Zinc Oxide
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Cyberderm Laboratories inc.

Guthy-Renker LLC

KAVI Skin Solutions, Inc.

NDC Product

Coral Kavi
NDC 42771-0001

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH FINAL
Inactive / Discontinued
NDC Product

Aqua Kavi
NDC 42771-0002

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH FINAL
Inactive / Discontinued

Marlex Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Hydrocortisone Acetate
NDC 10135-751

Generic Name
Hydrocortisone Acetate
Dosage Form
Suppository
Route
Rectal
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Meaningful Beauty, LLC

Neilmed Pharmaceuticals Inc.

NDC Product
Human Otc Drug

Bisacodyl Laxative
NDC 13709-328

Generic Name
Bisacodyl Laxative Suppositories
Dosage Form
Suppository
Route
Rectal
Marketing
OTC MONOGRAPH DRUG
Active Listing

Patrin Pharma Inc.

NDC Product
Human Prescription Drug

Hydrocortisone Acetate
NDC 39328-029

Generic Name
Hydrocortisone Acetate
Dosage Form
Suppository
Route
Rectal
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Hydrocortisone Acetate
NDC 39328-129

Generic Name
Hydrocortisone Acetate
Dosage Form
Suppository
Route
Rectal
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Rebel Distributors Corp

NDC Product

Hydrocortisone Acetate
NDC 21695-731

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

Ripar Cosmetici srl

NDC Product

Camouflage Concealer Cream
NDC 72399-100

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Camouflage Concealer Cream
NDC 72399-101

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Camouflage Concealer Cream
NDC 72399-102

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Camouflage Concealer Cream
NDC 72399-103

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Camouflage Concealer Cream
NDC 72399-104

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Camouflage Concealer Cream
NDC 72399-105

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Camouflage Concealer Cream
NDC 72399-106

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Camouflage Concealer Cream
NDC 72399-107

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-108

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-109

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-110

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-111

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-112

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-113

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-114

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-115

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-116

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-117

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-118

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-119

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-120

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-121

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-122

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-123

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-124

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-125

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-126

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-127

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-128

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-129

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-130

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Cover Cream. Sun Protection
NDC 72399-131

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

SHISEIDO AMERICAS CORPORATION

NDC Product
Human Otc Drug

Shiseido Future Lx Universal Defense S
NDC 58411-902

Generic Name
Octisalate, Octocrylene, And Zinc Oxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Salix Pharmaceuticals, Inc

NDC Product
Human Prescription Drug

Anusol Hc
NDC 65649-411

Generic Name
Hydrocortisone Acetate
Dosage Form
Suppository
Route
Rectal
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Proctocort
NDC 65649-511

Generic Name
Hydrocortisone Acetate
Dosage Form
Suppository
Route
Rectal
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Sandoz Inc

NDC Product
Human Prescription Drug

Hycamtin
NDC 66758-101

Generic Name
Topotecan
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Hycamtin
NDC 66758-102

Generic Name
Topotecan
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Unconditional Love d/b/a Hello Bello

NDC Product

Zinc Oxide
NDC 73418-010

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH FINAL
Inactive / Discontinued

External Clinical & Regulatory Resources

CAS
Common Chemistry
NCATS
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NLM
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NCATS
GSRS Full Record
NIH
NCI Thesaurus