NDC 62742-4166 Protect Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62742-4166?
What are the uses for Protect Broad Spectrum Spf 30?
Which are Protect Broad Spectrum 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)
Which are Protect Broad Spectrum 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- POLYHYDROXYSTEARIC ACID STEARATE (UNII: 8KQ7I65XZE)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ALOE (UNII: V5VD430YW9)
- PHORMIUM TENAX SEED OIL (UNII: OZ80CEA779)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- GARDENIA CORNUTA WHOLE (UNII: 0WC27VVS87)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PRUNUS AMERICANA FRUIT (UNII: 3F57WKW68K)
- HONEY (UNII: Y9H1V576FH)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TOTAROL (UNII: 67NH2854WW)
- FERULIC ACID (UNII: AVM951ZWST)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARRAGEENAN (UNII: 5C69YCD2YJ)
- PUNICA GRANATUM FLOWER (UNII: D9B634V4GP)
- CORN STARCH 3-E-DODECENYL SUCCINIC ANHYDRIDE MODIFIED (UNII: QG4MW19XYX)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ASTAXANTHIN (UNII: 8XPW32PR7I)
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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".