MOISTURIZING BODY- glycerin lotion 
MIGUHARA

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ACTIVE INGREDIENT

Active Ingredient: Glycerin 5.0%

INACTIVE INGREDIENT

Inactive Ingredients: Camellia Sinensis Leaf Extract, Ethylhexyl Palmitate, Kluyveromyces/Lactobacillus/Camellia Japonica Seed Oil Ferment Filtrate, Shea Butter Glycerides, Saccharomyces/Snail Secretion Filtrate Ferment Filtrate, Butylene Glycol, Polymethyl Methacrylate, Cetearyl Alcohol/Cetearyl Glucoside, 1,2-Hexanediol, Cetearyl Alcohol, Stearic Acid, Dimethicone, Tocopheryl Acetate, Sodium Hyaluronate, Allantoin, Aniba Rosaeodora (Rosewood) Wood Oil, Xanthan Gum, 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: After shower, dry yourself body with a towel and put the lotion on your body.

Usage

Usage: After shower, dry yourself body with a towel and put the lotion on your body.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

MOISTURIZING BODY 
glycerin lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70380-270
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin15 g  in 300 mL
Inactive Ingredients
Ingredient NameStrength
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
Ethylhexyl Palmitate (UNII: 2865993309)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70380-270-01300 mL in 1 CARTON; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/02/2016
Labeler - MIGUHARA (689204213)
Registrant - MIGUHARA (689204213)
Establishment
NameAddressID/FEIBusiness Operations
MIGUHARA689204213manufacture(70380-270)

Revised: 2/2016
Document Id: 45bc48f0-ae10-443d-84bb-0f156c49df13
Set id: 46482b91-f1d5-4f2e-8590-5db31860af7b
Version: 1
Effective Time: 20160223
 
MIGUHARA