Label: ULTRA WHITENING AMPLE- niacinamide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70380-320-01 - Packager: MIGUHARA
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 24, 2016
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Anthemis nobilis flower extract, Butylene glycol, Glycerin, Nelumbium speciosum flower extract, Iris versicolor extract, Gnaphalium leontopodium flower extract, Jasminum officinale(Jasmine) flower extract, Lilium candidum flower extract, Rosa centifolia flower extract, Freesia refracta extract, Sodium hyaluronate, Eclipta prostrata extract, Rehmannia glutinosa root extract, Artemisia princeps leaf extract, Portulaca oleracea extract, Glycyrrhiza glabra (Licorice) root extract, Lonicera japonica(Honeysuckle) flower extract, Zanthoxylum piperitum fruit extract, Pulsatilla koreana extract, Citrus paradisi(Grapefruit) fruit extract, Pentapeptide-13, Galactomyces ferment filtrate, Tremella fuciformis (Mushroom) extract, Glycosyl trehalose, Hydrogenated starch hydrolysate, PEG-60 hydrogenated castor oil, Hydroxyethylcellulose, Carbomer, Arginine, Xanthan gum, Gardenia florida fruit extract, Allantoin, Disodium EDTA, Citrus paradisi (Grapefruit) peel oil
- PURPOSE
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WARNINGS
Warnings:
1. Stop usage immediately if any of the below symptoms occur. Continued use could aggravate symptoms, so it is advisable to consult with a dermatologist immediately. 1) Symptoms include but not limited to: red spots, swelling, itchiness. 2) When having the same symptoms as above due to direct sunlight. 2. Do not apply to areas affected by dermatitis, eczema or wounds. 3. Storage and handling: 1) Tightly close lid after each use. 2 Keep out of reach of children 3) Store in a cool dry area, away from sunlight
- KEEP OUT OF REACH OF CHILDREN
- Usage
- Usage
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ULTRA WHITENING AMPLE
niacinamide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70380-320 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.7 g in 35 mL Inactive Ingredients Ingredient Name Strength CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG) Butylene glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70380-320-01 35 mL in 1 CARTON; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/02/2016 Labeler - MIGUHARA (689204213) Registrant - MIGUHARA (689204213) Establishment Name Address ID/FEI Business Operations MIGUHARA 689204213 manufacture(70380-320)
