NDC 70532-001 Elixir Fine Sunscreen Broad Spectrum Spf 15
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What is NDC 70532-001?
What are the uses for Elixir Fine Sunscreen Broad Spectrum Spf 15?
Which are Elixir Fine Sunscreen Broad Spectrum Spf 15 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)
Which are Elixir Fine Sunscreen Broad Spectrum 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)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PROPANEDIOL (UNII: 5965N8W85T)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- SUCROSE LAURATE (UNII: 05Q7CD0E49)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SUCROSE DILAURATE (UNII: 5926LC4S7M)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MARITIME PINE (UNII: 50JZ5Z98QY)
- ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- PALMITIC ACID (UNII: 2V16EO95H1)
- DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- URSOLIC ACID (UNII: P3M2575F3F)
- ALCOHOL (UNII: 3K9958V90M)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
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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".