APPLE BUBBLE- glycerin injectable foam 
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 10.0%

INACTIVE INGREDIENT

Inactive Ingredients: Aloe Barbadensis Leaf Water, Sodium Cocoyl, Apple Amino Acids, Sodium Lauroyl Aspartate, Hydrogenated Starch Hydrolysate, Glycosyl Trehalose, Pinus Palustris leaf extract, Citrus Grandis Seed Extract, Bambusa Textilis Stem Extract

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings:

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 4. Be aware not to get into eye.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Usage

Usage: Get decent amount of foam by pumping a container. Gently apply it along the skin texture as if massage is given and cleanse it.

Usage

Usage: Get decent amount of foam by pumping a container. Gently apply it along the skin texture as if massage is given and cleanse it.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

APPLE BUBBLE 
glycerin injectable foam
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70380-130
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin12 g  in 120 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70380-130-01120 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(70380-130)

Revised: 2/2016
Document Id: b89e4291-94d8-4335-879a-2a64a4ce304e
Set id: 45ab2f5c-bc41-4a9f-99b6-29517903af15
Version: 1
Effective Time: 20160219
 
MIGUHARA