Label: NOBLROSE FOAM CLEANSER- allantoin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60899-070-01 - Packager: AMAROS 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 April 11, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Sodium Laureth Sulfate, PEG-7 Glyceryl Cocoate, Cocamidopropyl Betain, Lauramide DEA, Glycerin, Butylene Glycol, Polysorbate20, Panthenol, Caprylyl Glycol, Caprylhydroxamic Acid, Rose Flower Oil, Disodium EDTA, CI 14700, Methylchloroisothiazolinone, Methylisothiazolinone Mixed Solution, Citric Acid, Fragrance.
- PURPOSE
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WARNINGS
Warnings: 1. In case of having following symptoms after using this product, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In case of getting it into your eyes, you have to wash it immediately.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
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DOSAGE AND ADMINISTRATION
Dosage and Administration: Foam Cleansing is a cleanser and make up remover in one. Wet your face with water. Pump 2 or 3 pumps of foaming cleanser into the palms of your hands. Rub the cleanser gently into your skin in circular motion with fingertips. Wash off the cleanser by splashing water onto your face. Dab face dry with a clean towel.
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NOBLROSE FOAM CLEANSER
allantoin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60899-070 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) Allantoin 0.75 mg in 150 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60899-070-01 150 mL in 1 CARTON; Type 0: Not a Combination Product 09/01/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 09/01/2013 Labeler - AMAROS CO., LTD. (690338801) Registrant - AMAROS CO., LTD. (690338801) Establishment Name Address ID/FEI Business Operations AMAROS CO., LTD. 690338801 manufacture(60899-070)