Label: OERBEUA SHINING MASK- glycerin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71342-0022-1 - Packager: DR.GLODERM
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 January 8, 2018
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
step 1:
after cleansing, apply the STEP 1 over dry facr for feeling the warmth
after 5 minutes, rinse well with warm water as if massaging
step 2:
after cleansing refine your skin with a toner
oper the STEP 2 and place the maks on your face
after 10~20 minutes, remove it and gently pat the remaining essence to promote absorption
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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 sunlight - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
OERBEUA SHINING MASK
glycerin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71342-0022 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 4.975 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PANTHENOL (UNII: WV9CM0O67Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71342-0022-1 210 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/09/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part347 01/09/2018 Labeler - DR.GLODERM (694773267) Registrant - DR.GLODERM (694773267) Establishment Name Address ID/FEI Business Operations ES COSMETICS 690422834 manufacture(71342-0022) Establishment Name Address ID/FEI Business Operations DR.GLODERM 694773267 label(71342-0022)
