Label: AN ADC SP INTENSIVE MOISTURE ESSENCE- niacinamide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69153-080-01, 69153-080-02 - Packager: AN 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 June 24, 2016
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Dipropylene Glycol, Phytosqualane, Glycerin, Phenyl Trimethicone, Panthenol, Cyclopentasiloxane/PEG-10 Dimethicone/Vinyl Dimechicone Cross Polymer, Cyclopentasiloxane, Hydrogenated Lecithin, 1,2-Hexanediol, Polyglyceryl-3 Methylglucose Distearate, Polyacrylamide/C13-14 Isoparaffin/ Laureth-7, CeramideNP/Hydrogenated Polydecene/Stearic Acid/ButyrospermumParkii(Shea) Butter/Ceteareth-20//Glyceryl Citrate/Lactate/Linoleate/Oleate Butylene glycol, Ethoxydiglycol, Trimethylpentanediol/Adipic Acid Copolymer, Sodium Polyacrylate, Phenoxyethanol, Beta-Glucan, Tocopheryl Acetate, Carbomer, Triethanolamine, Fragrance, Sodium Hyaluronate, Sodium Stearoyl Glutamate, Xanthan Gum, Disodium EDTA, Copper Tripeptide-1, Acetyl Hexapeptide-8, Palmitoyl Pentapeptide-4
- PURPOSE
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WARNINGS
Precautions on use: 1. Stop using the product if there are any of the following abnormal symptoms appearing after use and consult with your dermatologist as continued use can worsen the symptoms. A) If there are red spots, swelling, itchiness, or irritation B) If the above symptoms appear around the skin to which the product has been applied after being exposed to direct sunlight. 2. Precautions on storage and handling A) Make sure to close the cap after use. B) Keep out of the reach of children. C) Do not keep the product in a hot or cold place or a place getting direct sunlight. 3. Do not apply the product to any parts of the skin with wound, eczema, or dermatitis.
- KEEP OUT OF REACH OF CHILDREN
- Suggested use
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AN ADC SP INTENSIVE MOISTURE ESSENCE
niacinamide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69153-080 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.10 g in 55 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Dipropylene Glycol (UNII: E107L85C40) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69153-080-02 1 in 1 CARTON 05/01/2016 1 NDC:69153-080-01 55 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2016 Labeler - AN Co Ltd. (688448454) Registrant - AN Co Ltd. (688448454) Establishment Name Address ID/FEI Business Operations AN Co Ltd. 688448454 manufacture(69153-080)
