NDC 61995-2405 Al0040500 Alba Ve Mineral Sunscreen Herbal Fresh Spf35
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What is NDC 61995-2405?
What are the uses for Al0040500 Alba Ve Mineral Sunscreen Herbal Fresh Spf35?
Which are Al0040500 Alba Ve Mineral Sunscreen Herbal Fresh Spf35 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Al0040500 Alba Ve Mineral Sunscreen Herbal Fresh Spf35 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:
- LAVANDIN OIL (UNII: 9RES347CKG)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GINKGO (UNII: 19FUJ2C58T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)
- SPEARMINT OIL (UNII: C3M81465G5)
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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".