Label: ATONO2 OXYGEN BABY CREAM- glycerin cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70993-0011-1 - Packager: LAORGANIC Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 13, 2016
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Caprylic/Capric Triglyceride, Butylene Glycol, Butylene Glycol Dicaprylate/Dicaprate, Polyglyceryl-3 Methylglucose Distearate, Squalane, Dipropylene Glycol, Helianthus Annuus (Sunflower) Seed Oil, Beeswax, Cyclopentasiloxane, Sorbitan Stearate, Butyrospermum Parkii (Shea) Butter, Macadamia Integrifolia Seed Oil, Betaine, etc.
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
- For external use only
- When using this product
1. If any one of following symptoms occurs when using cosmetics, stop using it and consult a dermatologist.
A. red spot, swelling, itching, stimulus
B. symptoms mentioned above are caused by sunlight.2. Do not apply on skin where there is wound, eczema, or irritation.
3. Storage and cautions for handling
A. Close stopper after using.
B. Keep out of reach of children.
C. Keep away from high or low temperature and direct sunlight.4. This is not a medicinal product. Made of 100% cosmetic ingredients, it is a sensitive-skin care product for all skin types.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ATONO2 OXYGEN BABY CREAM
glycerin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70993-0011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 8.06 g in 100 g Inactive Ingredients Ingredient Name Strength SHEA BUTTER (UNII: K49155WL9Y) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70993-0011-1 160 g in 1 TUBE; Type 0: Not a Combination Product 09/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part347 10/01/2015 Labeler - LAORGANIC Co., Ltd. (689844148) Registrant - LAORGANIC Co., Ltd. (689844148) Establishment Name Address ID/FEI Business Operations LAORGANIC Co., Ltd. 689844148 manufacture(70993-0011)