NDC 69840-006 Yes To Natural Man Broad Spectrum Spf 15 Face
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69840-006?
What are the uses for Yes To Natural Man Broad Spectrum Spf 15 Face?
Which are Yes To Natural Man Broad Spectrum Spf 15 Face UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Yes To Natural Man Broad Spectrum Spf 15 Face 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)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ACETATE (UNII: 4Q43814HXS)
- PROPANEDIOL (UNII: 5965N8W85T)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- COCONUT OIL (UNII: Q9L0O73W7L)
- SHEA BUTTER (UNII: K49155WL9Y)
- COCOA BUTTER (UNII: 512OYT1CRR)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- SQUALANE (UNII: GW89575KF9)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ORANGE (UNII: 5EVU04N5QU)
- LIME PEEL (UNII: 544EQK5Q0W)
- MENTHA AQUATICA VAR. CITRATA LEAF (UNII: ZMA317E4J7)
- LEMON PEEL (UNII: 72O054U628)
- SOYBEAN OIL (UNII: 241ATL177A)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
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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".