NDC 54272-202 Firming Day Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 54272-202?
What are the uses for Firming Day Spf 30?
Which are Firming Day 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 Firming Day 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)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- 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)
- DIMETHICONE PEG-10 PHOSPHATE (UNII: O7Q5NJ7X88)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- DODECAMETHYLPENTASILOXANE (UNII: 0QDQ2VQ5YJ)
- 2,2,2-TRIFLUOROACETOPHENONE (UNII: 6T7L1UPY09)
- QUATERNIUM-91 (UNII: 00J8H295NB)
- BENTONITE (UNII: A3N5ZCN45C)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- 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".