NDC 52554-1111 Sunscreen 100
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 52554-1111?
What are the uses for Sunscreen 100?
Which are Sunscreen 100 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Sunscreen 100 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:
- JOJOBA OIL (UNII: 724GKU717M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SQUALANE (UNII: GW89575KF9)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PROPANEDIOL (UNII: 5965N8W85T)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- GLYCERIN (UNII: PDC6A3C0OX)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- DOCOSANOL (UNII: 9G1OE216XY)
- PURSLANE (UNII: M6S840WXG5)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SACCHARIDE HYDROLYSATE (UNII: ED959S6ACY)
- CHIA SEED (UNII: NU0OLX06F8)
- TURMERIC (UNII: 856YO1Z64F)
- WATER (UNII: 059QF0KO0R)
- DIBUTYL ADIPATE (UNII: F4K100DXP3)
- SUCROSE STEARATE (UNII: 274KW0O50M)
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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".