NDC 75936-207 Daily Correct Cc Cream Broad Sunscreen Spf 35 Light/medium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75936 - Taylor James Ltd
- 75936-207 - Daily Correct Cc Cream Broad Sunscreen Spf 35 Light/medium
Product Packages
NDC Code 75936-207-02
Package Description: 1 BOTTLE in 1 BOX / 47 mL in 1 BOTTLE (75936-207-01)
Product Details
What is NDC 75936-207?
What are the uses for Daily Correct Cc Cream Broad Sunscreen Spf 35 Light/medium?
Which are Daily Correct Cc Cream Broad Sunscreen Spf 35 Light/medium 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 OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Daily Correct Cc Cream Broad Sunscreen Spf 35 Light/medium 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)
- ISODODECANE (UNII: A8289P68Y2)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPANEDIOL (UNII: 5965N8W85T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- MICA (UNII: V8A1AW0880)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- APPLE (UNII: B423VGH5S9)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- 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".