EGF CRYSTAL 10 PPM- glycerin cream

EGF Crystal 10 ppm by

Drug Labeling and Warnings

EGF Crystal 10 ppm by is a Otc medication manufactured, distributed, or labeled by MIGUHARA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Glycerin 4.0%

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

Purpose: Skin Protectant

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

KEEP OUT OF REACH OF CHILDREN

Usage

Usage: Take an appropriate amount and gently apply it on the face.

Usage

Usage: Take an appropriate amount and gently apply it on the face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EGF CRYSTAL 10 PPM 
glycerin cream

Product 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)