NDC 70081-002 Sun Protective Day Moisturizer Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70081-002?
What are the uses for Sun Protective Day Moisturizer Sunscreen?
Which are Sun Protective Day Moisturizer Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Sun Protective Day Moisturizer Sunscreen 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)
- ACACIA DECURRENS WHOLE (UNII: 8KZ75S2VSK)
- JOJOBA OIL (UNII: 724GKU717M)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- GLYCERIN (UNII: PDC6A3C0OX)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- CREATININE (UNII: AYI8EX34EU)
- ADANSONIA DIGITATA SEED OIL (UNII: 77MKL7AR5I)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8)
- BETAINE (UNII: 3SCV180C9W)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TOCOPHEROL (UNII: R0ZB2556P8)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- LAURETH-7 (UNII: Z95S6G8201)
- BARLEY (UNII: 5PWM7YLI7R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- DISODIUM RUTINYL DISULFATE (UNII: V5J3537PND)
- ETHYLBISIMINOMETHYLGUAIACOL MANGANESE CHLORIDE (UNII: SM5YJ88LTU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
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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".