NDC 24979-144 Hydroquinone Time Release
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What is NDC 24979-144?
What are the uses for Hydroquinone Time Release?
Which are Hydroquinone Time Release UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Hydroquinone Time Release 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:
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- LEVOMENOL (UNII: 24WE03BX2T)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLOXAMER 188 (UNII: LQA7B6G8JG)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- WATER (UNII: 059QF0KO0R)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SORBITAN TRISTEARATE (UNII: 6LUM696811)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRICONTANYL POVIDONE (UNII: N0SS3Q238D)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Hydroquinone Time Release?
- RxCUI: 197795 - hydroquinone 4 % Topical Cream
- RxCUI: 197795 - hydroquinone 40 MG/ML Topical Cream
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".