RE-ACTION E- bambusa arundinacea stem extract,maltodextrin,aloe barbadensis leaf juice,caffeine powder

Re-action E by

Drug Labeling and Warnings

Re-action E by is a Otc medication manufactured, distributed, or labeled by Goldeneye Permanent System GmbH Germany, Hanaim International Llc, Goldeneye Permanent System Gmbh Germany. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Bambusa Arundinacea Stem Extract (10%)

Maltodextrin (2.98%)

Aloe Barbadensis Leaf Juice (0.5%)

Caffeine (0.2%)

Purpose

Skin exfoliate

Keep out of reach of children

Do not swallow. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Warnings

For external use only
Do not use when Your skin is red, inflamed, irritated or painful
When using this product
 Do not apply on other parts of the body
 Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
 Do not apply directly to wound or open cut.
Stop use and ask doctor if rash or irritation on skin develops and lasts.
Keep out of reach of children
 Do not swallow. In case of accidental ingestion, seek professional assistance.
Store at room temperature

Uses

For enzymatic and mechanical facial skin peeling. Keep skin soft and smooth.

Directions

Cleanse your face. Do not dry your skin after cleansing. Apply Re-action E with fingertips and massage the moist skin in a circular motion. Applicable on face, neck and decollete. Avoid the eye and mouth area. Leave it on for at least 5 minutes before rinsing off with lukewarm water

Inactive Ingredients

Sodium Lauroyl Glutamate, Sodium Cocoyl Glycinate, Synthetic Fluro phlogopite, Argania Spinosa Shell Powder, Persea Gratissima (Avocado) Oil, Subtilisin, Lipase

bdr Re-action E

INGREDIENTS AND APPEARANCE

RE-ACTION E 
bambusa arundinacea stem extract,maltodextrin,aloe barbadensis leaf juice,caffeine powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71056-117
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MALTODEXTRIN (UNII: 7CVR7L4A2D) (MALTODEXTRIN - UNII:7CVR7L4A2D)	MALTODEXTRIN	0.012 g  in 0.4 g
BAMBUSA ARUNDINACEA STEM (UNII: NRA4497HC5) (BAMBUSA ARUNDINACEA STEM - UNII:NRA4497HC5)	BAMBUSA ARUNDINACEA STEM	0.04 g  in 0.4 g
ALOE VERA LEAF (UNII: ZY81Z83H0X) (ALOE VERA LEAF - UNII:ZY81Z83H0X)	ALOE VERA LEAF	0.0007 g  in 0.4 g
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E)	CAFFEINE	0.0008 g  in 0.4 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM COCOYL GLYCINATE (UNII: XLU9KH03XM)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71056-117-02	12 in 1 CARTON	07/27/2018
1	NDC: 71056-117-01	0.4 g in 1 AMPULE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/27/2018

Labeler - Goldeneye Permanent System GmbH Germany (329178144)

Registrant - Hanaim International Llc (070319425)

Establishment
Name	Address	ID/FEI	Business Operations
Goldeneye Permanent System Gmbh Germany		329178144	manufacture(71056-117)