NDC 24488-004 Revitol Acne Treatment
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 24488-004?
What are the uses for Revitol Acne Treatment?
Which are Revitol Acne Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOIC ACID (UNII: 8SKN0B0MIM) (Active Moiety)
Which are Revitol Acne Treatment 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- ALLANTOIN (UNII: 344S277G0Z)
- TROLAMINE (UNII: 9O3K93S3TK)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TEA TREE OIL (UNII: VIF565UC2G)
- BETULA PUBESCENS RESIN (UNII: 9G931M6I4G)
- EPILOBIUM ANGUSTIFOLIUM LEAF (UNII: 7NV86426N2)
- BILBERRY (UNII: 9P2U39H18W)
- SUGARCANE (UNII: 81H2R5AOH3)
- ORANGE (UNII: 5EVU04N5QU)
- LEMON PEEL (UNII: 72O054U628)
- SAGE (UNII: 065C5D077J)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HONEY (UNII: Y9H1V576FH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Revitol Acne Treatment?
- RxCUI: 1112691 - Revitol 5 % Topical Cream
- RxCUI: 1112691 - benzoyl peroxide 50 MG/ML Topical Cream [Revitol]
- RxCUI: 1112691 - Revitol 50 MG/ML Topical Cream
- RxCUI: 308693 - benzoyl peroxide 5 % Topical Cream
- RxCUI: 308693 - benzoyl peroxide 50 MG/ML Topical Cream
* Please review the disclaimer below.
[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".