NDC 61995-2765 Alba Acnedote Clean Treat Towelette
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What is NDC 61995-2765?
What are the uses for Alba Acnedote Clean Treat Towelette?
Which are Alba Acnedote Clean Treat Towelette UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Alba Acnedote Clean Treat Towelette 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:
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ORANGE OIL (UNII: AKN3KSD11B)
- PROPANEDIOL (UNII: 5965N8W85T)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
- PARSLEY (UNII: 58FMD0Q0EV)
- CHAMOMILE (UNII: FGL3685T2X)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Alba Acnedote Clean Treat Towelette?
- RxCUI: 797892 - salicylic acid 2 % Medicated Pad
- RxCUI: 797892 - salicylic acid 20 MG/ML Medicated Pad
- RxCUI: 797892 - salicylic acid 2 % Topical Swab
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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".