NDC 71623-100 Natural Friend White Day Soft Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71623 - Asia Nanotech Co., Ltd.
- 71623-100 - Natural Friend White Day Soft Cream
Product Packages
NDC Code 71623-100-02
Package Description: 1 CONTAINER in 1 PACKAGE / 50 g in 1 CONTAINER (71623-100-01)
Product Details
What is NDC 71623-100?
What are the uses for Natural Friend White Day Soft Cream?
Which are Natural Friend White Day Soft Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Natural Friend White Day Soft Cream 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)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- FU LING (UNII: XH37TWY5O4)
- REISHI (UNII: TKD8LH0X2Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- HONEY (UNII: Y9H1V576FH)
- PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)
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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".