BDR RE-CHARGE N HYDRO SERUM MAXIMUM SKIN ENERGIZER- panthenol 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-charge N hydro serum maximum skin energizer

Active Ingredients

Panthenol (1.5%)

Purpose

Skin protectant

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

Moisturizes and keeps skin soft and smooth. Suitable for the delicate eye area.

Directions

Apply 1-2 dosage units and massage over entire area.

Inactive Ingredients

AQUA (WATER), GLYCERIN, HYDROXYPROPYL CYCLODEXTRIN, SODIUM LACTATE, SODIUM PCA, HYDROXYETHYL CELLULOSE, PHENOXYETHANOL, DISODIUM ADENOSINE TRIPHOSPHATE, PENTYLENE GLYCOL, BENZOIC ACID, SODIUM HYALURONATE, DEHYDROACETIC ACID, SODIUM HYDROXIDE, CARICA PAPAYA (PAPAYA) FRUIT EXTRACT, ALGIN, SODIUM PHYTATE, UREA, FRUCTOSE, GLYCINE

bdr Re-charge N hydro serum maximum skin energizer

Recharge n energizer

BDR RE-CHARGE N HYDRO SERUM MAXIMUM SKIN ENERGIZER 
panthenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71056-105
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL0.45 g  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PAPAYA (UNII: KU94FIY6JB)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
PHYTATE SODIUM (UNII: 88496G1ERL)  
UREA (UNII: 8W8T17847W)  
FRUCTOSE (UNII: 6YSS42VSEV)  
GLYCINE (UNII: TE7660XO1C)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71056-105-021 in 1 PACKAGE11/15/201604/14/2021
1NDC:71056-105-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/15/201604/14/2021
Labeler - Goldeneye Permanent System Gmbh Germany (329178144)
Establishment
NameAddressID/FEIBusiness Operations
Goldeneye Permanent System Gmbh Germany329178144manufacture(71056-105)

Revised: 5/2021
 
Goldeneye Permanent System Gmbh Germany