NDC 54272-201 Brighten Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 54272-201?
What are the uses for Brighten Spf 30?
Which are Brighten Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Brighten Spf 30 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CORALLINA OFFICINALIS (UNII: 4004498D06)
- PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
- OAT (UNII: Z6J799EAJK)
- ANGELICA SINENSIS WHOLE (UNII: 697D19QDBN)
- 10-HYDROXYDECANOIC ACID (UNII: NP03XO416B)
- SEBACIC ACID (UNII: 97AN39ICTC)
- 1,10-DECANEDIOL (UNII: 5I577UDK52)
- BETAINE (UNII: 3SCV180C9W)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
- PROLINE (UNII: 9DLQ4CIU6V)
- ALANINE (UNII: OF5P57N2ZX)
- SERINE (UNII: 452VLY9402)
- MAGNESIUM LACTATE (UNII: MT6QI8324A)
- POTASSIUM LACTATE (UNII: 87V1KMK4QV)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SORBIC ACID (UNII: X045WJ989B)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
* Please review the disclaimer below.
[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".