NDC 75936-202 Cc Cream Broad Spectrum Sunscreen Spf 35 Fair To Light
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75936 - Taylor James Ltd
- 75936-202 - Cc Cream Broad Spectrum Sunscreen Spf 35 Fair To Light
Product Packages
NDC Code 75936-202-02
Package Description: 1 BOTTLE in 1 BOX / 47 mL in 1 BOTTLE (75936-202-01)
Product Details
What is NDC 75936-202?
What are the uses for Cc Cream Broad Spectrum Sunscreen Spf 35 Fair To Light?
Which are Cc Cream Broad Spectrum Sunscreen Spf 35 Fair To Light UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Cc Cream Broad Spectrum Sunscreen Spf 35 Fair To Light 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ISODODECANE (UNII: A8289P68Y2)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPANEDIOL (UNII: 5965N8W85T)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- APPLE (UNII: B423VGH5S9)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MICA (UNII: V8A1AW0880)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
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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".