NDC 61995-2796 Alba Botanica Fast Fix For Pimple
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What is NDC 61995-2796?
What are the uses for Alba Botanica Fast Fix For Pimple?
Which are Alba Botanica Fast Fix For Pimple UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Alba Botanica Fast Fix For Pimple 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- BROWN IRON OXIDE (UNII: 1N032N7MFO)
- ISOAMYL LAURATE (UNII: M1SLX00M3M)
- SORBITOL (UNII: 506T60A25R)
- ALCOHOL (UNII: 3K9958V90M)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- CETYL ALCOHOL (UNII: 936JST6JCN)
What is the NDC to RxNorm Crosswalk for Alba Botanica Fast Fix For Pimple?
- RxCUI: 417462 - sulfur 6 % Topical Cream
- RxCUI: 417462 - sulfur 60 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".