NDC 98132-725 Bareminerals Blemish Therapy
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What is NDC 98132-725?
What are the uses for Bareminerals Blemish Therapy?
Which are Bareminerals Blemish Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Bareminerals Blemish Therapy 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:
- ZINC STEARATE (UNII: H92E6QA4FV)
- BARIUM SULFATE (UNII: 25BB7EKE2E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- KAOLIN (UNII: 24H4NWX5CO)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- BETAINE SALICYLATE (UNII: DRF395F9AY)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TEA TREE OIL (UNII: VIF565UC2G)
- PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- RETINOL (UNII: G2SH0XKK91)
- ICODEXTRIN (UNII: 2NX48Z0A9G)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- FARNESOL (UNII: EB41QIU6JL)
- NIACINAMIDE (UNII: 25X51I8RD4)
- MAGNESIUM MYRISTATE (UNII: Z1917F0578)
- MICA (UNII: V8A1AW0880)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Bareminerals Blemish Therapy?
- RxCUI: 1191710 - sulfur 3 % Topical Powder
- RxCUI: 1191710 - sulfur 0.03 MG/MG Topical Powder
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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".