Label: ISLEAF SHINE SMOOTH LIP GLAZE SOFT PINK- mineral oil liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 70818-010-01 - Packager: C3 Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 August 28, 2017
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
1) Occurrence of red spots, swelling, itchiness, and other skin irritation
2) If the symptoms above occur after the application area is exposed to direct sunlight
2. Do not use on open wounds, eczema, and other skin irritations
3. Precaution for Storage and Handling
1) Close the lid after use
2) Keep out of reach of infants and children
3) Do not to store in a place with high/low temperature and exposed to direct sunlight4. Use as avoiding eye areas.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ISLEAF SHINE SMOOTH LIP GLAZE SOFT PINK
mineral oil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70818-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL 8 g in 100 mL Inactive Ingredients Ingredient Name Strength SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) 2 g in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70818-010-01 2.5 mL in 1 APPLICATOR; Type 0: Not a Combination Product 08/08/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 08/08/2017 Labeler - C3 Co., Ltd. (689846633) Registrant - C3 Co., Ltd. (689846633) Establishment Name Address ID/FEI Business Operations C3 Co., Ltd. 689846633 label(70818-010) , pack(70818-010) , manufacture(70818-010)
