BDR RE-CHARGE N HYDRO SERUM MAXIMUM SKIN ENERGIZER- panthenol liquid

bdr Re-charge N hydro serum maximum skin energizer by

Drug Labeling and Warnings

bdr Re-charge N hydro serum maximum skin energizer by is a Otc medication manufactured, distributed, or labeled by Goldeneye Permanent System Gmbh Germany, Hanaim International Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

BDR RE-CHARGE N HYDRO SERUM MAXIMUM SKIN ENERGIZER 
panthenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71056-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z)	PANTHENOL	0.45 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71056-105-02	1 in 1 PACKAGE	11/15/2016
1	NDC: 71056-105-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/15/2016

Labeler - Hanaim International Llc (070319425)

Registrant - Hanaim International Llc (070319425)

Establishment
Name	Address	ID/FEI	Business Operations
Hanaim International Llc		070319425	relabel(71056-105)

Establishment
Name	Address	ID/FEI	Business Operations
Goldeneye Permanent System Gmbh Germany		329178144	manufacture(71056-105)