NDC 58633-269 Clarifying Colloidal Sulfur Mask
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58633-269?
What are the uses for Clarifying Colloidal Sulfur Mask?
Which are Clarifying Colloidal Sulfur Mask UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Clarifying Colloidal Sulfur Mask 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)
- KAOLIN (UNII: 24H4NWX5CO)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-100 STEARATE (UNII: YD01N1999R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- BENTONITE (UNII: A3N5ZCN45C)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- OPUNTIA TUNA FLOWERING TOP (UNII: R4AS8333O2)
- ALLANTOIN (UNII: 344S277G0Z)
- LEVOMENOL (UNII: 24WE03BX2T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- PHENYLETHYL RESORCINOL (UNII: G37UFG162O)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SOYBEAN OIL (UNII: 241ATL177A)
- FARNESOL (UNII: EB41QIU6JL)
- RETINOL (UNII: G2SH0XKK91)
What is the NDC to RxNorm Crosswalk for Clarifying Colloidal Sulfur Mask?
- RxCUI: 198871 - sulfur 5 % Topical Cream
- RxCUI: 198871 - sulfur 50 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".