NDC 75936-256 Body Butter Broad Spectrum Sunscreen Spf 40
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75936 - Taylor James Ltd.
- 75936-256 - Body Butter Broad Spectrum Sunscreen Spf 40
Product Packages
NDC Code 75936-256-01
Package Description: 168 mL in 1 PACKAGE
Product Details
What is NDC 75936-256?
What are the uses for Body Butter Broad Spectrum Sunscreen Spf 40?
Which are Body Butter Broad Spectrum Sunscreen Spf 40 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Body Butter Broad Spectrum Sunscreen Spf 40 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)
- ISODODECANE (UNII: A8289P68Y2)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRIMETHOXYBENZYLIDENE PENTANEDIONE (UNII: 322V0ACF25)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- RICE BRAN (UNII: R60QEP13IC)
- SUCROSE STEARATE (UNII: 274KW0O50M)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ROSEMARY (UNII: IJ67X351P9)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- HIPPOPHAE RHAMNOIDES SEED OIL (UNII: T53SBG6741)
- MANDARIN OIL (UNII: NJO720F72R)
- CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)
- CARDAMOM OIL (UNII: JM0KJ091HZ)
- CLOVE LEAF OIL (UNII: VCA5491KVF)
- CHINESE CINNAMON LEAF OIL (UNII: 4U4V2F2E4Y)
- VANILLIN (UNII: CHI530446X)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- LAVANDIN OIL (UNII: 9RES347CKG)
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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".