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bdr Re-fresh gel mask face

Medically reviewed on Nov 29, 2016

Dosage form: patch
Ingredients: Allantoin 0.12g in 60g
Labeler: Hanaim International Llc
NDC Code: 71056-112

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.

bdr Re-fresh gel mask face

Active Ingredients

Allantoin (0.2%)

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 helps gently calm stressed skin. Keep skin smooth and soft. Wrinkle care.

Directions

Apply on cleansed face for 10-15 minutes. After removing mask no need cleansing is required. Single use only.

Inactive Ingredients

AQUA (WATER), GLYCERIN, PROPYLENE GLYCOL, CORN GLUTEN AMINO ACIDS, COLLAGEN, ALLANTOIN, HYALURONIC ACID, PORTULACA OLERACEA EXTRACT, SH­ OLIGOPEPTIDE-1, UBIQUINONE (Q10), MICA, PHENOXYETHANOL, PARFUM

bdr Re-fresh gel mask face

BDR RE-FRESH GEL MASK FACE 
allantoin patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71056-112
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Allantoin (ALLANTOIN) Allantoin0.12 g  in 60 g
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
PROPYLENE GLYCOL 
AMINO ACIDS, CORN GLUTEN 
BOVINE TYPE I COLLAGEN 
HYALURONIC ACID 
PURSLANE 
UBIDECARENONE 
MICA 
PHENOXYETHANOL 
Packaging
#Item CodePackage Description
1NDC:71056-112-025 PATCH in 1 PACKAGE
1NDC:71056-112-0160 g in 1 PATCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/18/2016
Labeler - Hanaim International Llc (070319425)
Registrant - Hanaim International Llc (070319425)
Establishment
NameAddressID/FEIOperations
Hanaim International Llc070319425relabel(71056-112)
Establishment
NameAddressID/FEIOperations
Goldeneye Permanent System Gmbh Germany329178144manufacture(71056-112)

 
Hanaim International Llc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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