NDC 69435-1904 Gold Cosmetics Adi Clear
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69435 - Peer Pharm Ltd
- 69435-1904 - Gold Cosmetics Adi Clear
Product Packages
NDC Code 69435-1904-1
Package Description: 30 mL in 1 TUBE
Product Details
What is NDC 69435-1904?
What are the uses for Gold Cosmetics Adi Clear?
Which are Gold Cosmetics Adi Clear UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Gold Cosmetics Adi Clear 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- JOJOBA OIL (UNII: 724GKU717M)
- DECYL OLEATE (UNII: ZGR06DO97T)
- SODIUM DITHIONATE (UNII: RPF7Z41GAW)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- WATER (UNII: 059QF0KO0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETEARETH-30 (UNII: 1R9DCZ5FOX)
- STEARETH-21 (UNII: 53J3F32P58)
- STEARETH-2 (UNII: V56DFE46J5)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALLANTOIN (UNII: 344S277G0Z)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
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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".