Label: LUMINANT UMBRELLA MASK PACK- allantoin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 70098-0002-1 - Packager: GK COSMETIC 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 December 6, 2019
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENTallantoin
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INACTIVE INGREDIENTglycerin, butylene glycol, etc.
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PURPOSEskin protectant
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KEEP OUT OF REACH OF CHILDRENkeep out of reach of the children
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INDICATIONS & USAGE1. After wash your face, take our STEP01 - Luminant Umbrella Facial Mask and put it on your face. 2. Take off the sheet after 15 to 20 - minutes when it gets absorbed into your skin - 3. Tap your skin ...
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WARNINGS1. Do not use in the following cases(Eczema and scalp wounds) 2.Side Effects - 1)Due - to the use of this druf if rash, irritation, itching and symptopms of - hypersnesitivity ...
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DOSAGE & ADMINISTRATIONfor external use only
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information