NDC 24765-109 Cellzyme Secret Therapy
Glycerin, Hydroxyethyl Ethylcellulose , Allantoin Liquid Topical - View Dosage, Usage, Ingredients, Routes, UNII
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Code Structure Chart
Product Details
What is NDC 24765-109?
What are the uses for Cellzyme Secret Therapy?
What are Cellzyme Secret Therapy Active Ingredients?
- ALLANTOIN .145 g/100mL - A urea hydantoin that is found in URINE and PLANTS and is used in dermatological preparations.
- GLYCERIN 5.2 g/100mL
- HYDROXYETHYL ETHYLCELLULOSE 1.925 g/100mL
Which are Cellzyme Secret Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- HYDROXYETHYL ETHYLCELLULOSE (UNII: ZDN57Z154K)
- HYDROXYETHYL ETHYLCELLULOSE (UNII: ZDN57Z154K) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Cellzyme Secret Therapy Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- ARGININE (UNII: 94ZLA3W45F)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- JOJOBA OIL (UNII: 724GKU717M)
- SQUALANE (UNII: GW89575KF9)
- PROPANEDIOL (UNII: 5965N8W85T)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- PREZATIDE COPPER (UNII: 6BJQ43T1I9)
- NEPIDERMIN (UNII: TZK30RF92W)
- DATE (UNII: H3O7QI5HY7)
- FIG (UNII: TGD87RII2U)
- OPUNTIA COCHENILLIFERA FRUIT (UNII: 838ZTK02KH)
- OPUNTIA FICUS-INDICA (UNII: 23Z87HTQ6P)
- ADANSONIA DIGITATA SEED (UNII: 2936P60TPX)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- ARTEMISIA MONTANA LEAF (UNII: 1548S9624V)
- GINKGO (UNII: 19FUJ2C58T)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
Which are the Pharmacologic Classes for Cellzyme Secret Therapy?
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".