BDR RE-ACTION DEEP LOW BASE SKIN REFINER EXFOLIATION ESSENCE- glycolic acid liquid 
Goldeneye Permanent System Gmbh Germany

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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GOLDENEYE - bdr Re-action deep low base skin refiner exfoliation essence

Active Ingredients

Glycolic Acid (10%)

Purpose

Anti-wrinkle

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

Helps to remove dead skin cells gently, and improve skin texture to look radiant and fresh. For large-pored, oily, sensitive skin.

Directions

Apply 4-6 pumps on clean skin for 10-15 minutes. Rinse thoroughly with water. Use 1-3 times per week. Avoid contact with mucous membranes.

Inactive Ingredients

AQUA, SODIUM HYDROXIDE, CARBOXYMETHYL HYDROXYETHYL CELLULOSE, PROPYLENE GLYCOL, ARCTIUM LAPPA FRUIT EXTRACT, BIOTIN, ZINC PCA, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN

bdr Re-action deep low base skin refiner exfoliation essence

Reaction Deep

BDR RE-ACTION DEEP LOW BASE SKIN REFINER EXFOLIATION ESSENCE 
glycolic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71056-103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC ACID3 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ARCTIUM LAPPA FRUIT (UNII: EA541308MV)  
BIOTIN (UNII: 6SO6U10H04)  
ZINC PIDOLATE (UNII: C32PQ86DH4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71056-103-021 in 1 PACKAGE11/14/201604/12/2021
1NDC:71056-103-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/14/201604/12/2021
Labeler - Goldeneye Permanent System Gmbh Germany (329178144)
Registrant - Goldeneye Permanent System Gmbh Germany (329178144)
Establishment
NameAddressID/FEIBusiness Operations
Goldeneye Permanent System Gmbh Germany329178144manufacture(71056-103)

Revised: 5/2021
 
Goldeneye Permanent System Gmbh Germany