Label: MOISTURIZING BODY- glycerin lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 70380-270-01 - Packager: MIGUHARA
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 23, 2016
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Camellia Sinensis Leaf Extract, Ethylhexyl Palmitate, Kluyveromyces/Lactobacillus/Camellia Japonica Seed Oil Ferment Filtrate, Shea Butter Glycerides, Saccharomyces/Snail Secretion Filtrate Ferment Filtrate, Butylene Glycol, Polymethyl Methacrylate, Cetearyl Alcohol/Cetearyl Glucoside, 1,2-Hexanediol, Cetearyl Alcohol, Stearic Acid, Dimethicone, Tocopheryl Acetate, Sodium Hyaluronate, Allantoin, Aniba Rosaeodora (Rosewood) Wood Oil, Xanthan Gum, Disodium EDTA
- PURPOSE
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WARNINGS
Warnings:
1. Stop usage immediately if any of the below symptoms occur. Continued use could aggravate symptoms, so it is advisable to consult with a dermatologist immediately. 1) Symptoms include but not limited to: red spots, swelling, itchiness. 2) When having the same symptoms as above due to direct sunlight. 2. Do not apply to areas affected by dermatitis, eczema or wounds. 3. Storage and handling: 1) Tightly close lid after each use. 2 Keep out of reach of children 3) Store in a cool dry area, away from sunlight
- KEEP OUT OF REACH OF CHILDREN
- Usage
- Usage
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MOISTURIZING BODY
glycerin lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70380-270 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin 15 g in 300 mL Inactive Ingredients Ingredient Name Strength GREEN TEA LEAF (UNII: W2ZU1RY8B0) Ethylhexyl Palmitate (UNII: 2865993309) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70380-270-01 300 mL in 1 CARTON; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/02/2016 Labeler - MIGUHARA (689204213) Registrant - MIGUHARA (689204213) Establishment Name Address ID/FEI Business Operations MIGUHARA 689204213 manufacture(70380-270)
