NDC 76026-304 Puristics Totallyageless Spf 15 Daily Anti-aging
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What is NDC 76026-304?
What are the uses for Puristics Totallyageless Spf 15 Daily Anti-aging?
Which are Puristics Totallyageless Spf 15 Daily Anti-aging UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Puristics Totallyageless Spf 15 Daily Anti-aging 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SQUALANE (UNII: GW89575KF9)
- GLYCERIN (UNII: PDC6A3C0OX)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- SUCROSE DISTEARATE (UNII: 96QS1D0T15)
- SUCROSE STEARATE (UNII: 274KW0O50M)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- ELAEIS GUINEENSIS FRUIT BUTTER (UNII: UYH3R74N56)
- HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LAURIC ACID (UNII: 1160N9NU9U)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- RICE BRAN (UNII: R60QEP13IC)
- ALLANTOIN (UNII: 344S277G0Z)
- ROSEWOOD OIL (UNII: F2522O5L7B)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PANTHENOL (UNII: WV9CM0O67Z)
- HYALURONIC ACID (UNII: S270N0TRQY)
- LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
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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".