NDC 0363-8410 Studio35 Extra Strength Medicated Body
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 0363-8410?
What are the uses for Studio35 Extra Strength Medicated Body?
Which are Studio35 Extra Strength Medicated Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Studio35 Extra Strength Medicated Body 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)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: W6000VEI5Y)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- PETROLATUM (UNII: 4T6H12BN9U)
- STEARETH-21 (UNII: 53J3F32P58)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARETH-2 (UNII: V56DFE46J5)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
- XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
- ANHYDROXYLITOL (UNII: 8XWR7NN42F)
- XYLITOL (UNII: VCQ006KQ1E)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Studio35 Extra Strength Medicated Body?
- RxCUI: 1053386 - dimethicone 5 % / menthol 0.5 % Topical Lotion
- RxCUI: 1053386 - dimethicone 50 MG/ML / menthol 5 MG/ML Topical Lotion
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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".