NDC 55789-2403 Bronzing Mineral Beauty Balm Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 55789-2403?
What are the uses for Bronzing Mineral Beauty Balm Spf 15?
Which are Bronzing Mineral Beauty Balm Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Bronzing Mineral Beauty Balm Spf 15 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)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TOCOPHEROL (UNII: R0ZB2556P8)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYETHYL CELLULOSE (3000 MPA.S AT 1%) (UNII: 7Q6P4JN1QT)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ALCOHOL (UNII: 3K9958V90M)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SHEA BUTTER (UNII: K49155WL9Y)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839)
- ROSA CANINA FLOWER OIL (UNII: DUY7M48I1T)
- GINKGO (UNII: 19FUJ2C58T)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- THYME (UNII: CW657OBU4N)
- POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
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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".