Label: EGF CRYSTAL 10 PPM- glycerin cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70380-180-01 - Packager: MIGUHARA
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 22, 2016
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Streptomyces Subrutilus Ferment Filtrate Extract, Human Oligopeptide-1, Sodium Hyaluronate, Beta-Glucan, Lactobacillus/Dioscorea Japonica Root Extract Ferment Filtrate, 1,2-Hexanediol, Hydroxyethyl Ethylcellulose, Acetyl Hexapeptide-8, Palmitoyl Tripeptide-1, Piper Methysticum Leaf/Root/Stem Extract, Xanthan Gum, Adenosine, Disodium EDTA
- 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
EGF CRYSTAL 10 PPM
glycerin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70380-180 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin 1.0 g in 25 mL Inactive Ingredients Ingredient Name Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) 1,2-Hexanediol (UNII: TR046Y3K1G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70380-180-01 25 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(70380-180)
