Label: NATURAL FRIEND WHITE DAY SOFT CREAM- niacinamide, dimethicone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71623-100-01, 71623-100-02 - Packager: Asia Nanotech Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 14, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
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Warnings
For external use only
Do not use when skin is red, inflamed, irritated, or painful
When using this product
- do not apply on other parts of the body
- avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water
- do not apply directly to wound or open cut
Stop use and ask a doctor if
- Rash or irritation on skin develops and lasts
- Keep out of reach of children
- Directions
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Inactive Ingredients
Water, Butylene Glycol, Cyclomethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, 1,2-Hexanediol, Cetyl Ethylhexanoate, Titanium Dioxide, Aluminium Hydroxide, Triethoxycaprylylsilane, Sodium Chloride, Polyglutamic Acid, Phenoxyethanol, Potulaca Acidissima Extract, Cellulose, Rehmannia Glutinosa Root Extract, Panax Ginseng Root Extract, Poria Cocos Extract, Honey Extract, Ganoderma Lucidum (Mushroom) Extract, Camellia Sinensis Leaf Extract, Pinus Densiflora Leaf Extract, Fragrance
- Natural Friend White Day Soft Cream
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INGREDIENTS AND APPEARANCE
NATURAL FRIEND WHITE DAY SOFT CREAM
niacinamide, dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71623-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 1 g in 50 g DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 0.52 g in 50 g Inactive Ingredients Ingredient Name Strength 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71623-100-02 1 in 1 PACKAGE 07/26/2017 1 NDC:71623-100-01 50 g in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/26/2017 Labeler - Asia Nanotech Co., Ltd. (694056074) Registrant - Asia Nanotech Co., Ltd. (694056074) Establishment Name Address ID/FEI Business Operations Natuzen Co., Ltd 688201272 manufacture(71623-100) Establishment Name Address ID/FEI Business Operations Asia Nanotech Co., Ltd. 694056074 relabel(71623-100)
