Medication Guide App

IONTOPHORESIS ANTI AGING SOLUTION I

Dosage form: lotion
Ingredients: ALLANTOIN 0.1mL in 20mL
Labeler: ROCKET ELECTRIC CO., LTD.
NDC Code: 51985-010

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active Ingredient: Allantoin

Inactive Ingredients:
WATER, DIPROPYLENE GLYCOL, GLYCERIN, GLYCERYL POLYACRYLATE, DIETHOXYETHYL SUCCINATE, SODIUM HYALURONATE, PHENOXYETHANOL, ARGININE, CARBOMER,
PHENYL TRIMETHICONE, METHYLPARABEN, CAMELLIA SINENSIS LEAF EXTRACT, PEG-40 HYDROGENATED CASTOR OIL, PPG-26-BUTETH-26, XANTHAN GUM, DIPOTASSIUM GLYCYRRHIZATE, FRAGRANCE, ADENOSINE, DISODIUM EDTA, ACTINIDIA CHINENSIS (KIWI) FRUIT EXTRACT, BACILLUS/SOYBEAN FERMENT EXTRACT, GINKO BILOBA LEAF EXTRACT, HUMAN OLIGOPEPTIDE-1, SALIX ALBA (WILLOW) BARK EXTRACT, SOLUBLE COLLAGEN

Purpose:
For the treatment of wrinkles or for anti aging just 1 hour before you want to look younger.

Wanrings:
For external use only.
Avoid eye contact.
Do not use on damage skin.
Stop use consult a doctor if excess skin irritation develops and increases.

Keep out of reach of children:
If swallowed, get medical help right away.

Directions:
Apply Anti aging serum and pat gently for about a minute.
Peel patch from liner and turn over. black side onto skin.
Place patch around eye and leave on for 1 hour then remove.

Dosage and administration:
Apply Anti aging serum and pat gently for about a minute.
Peel patch from liner and turn over. black side onto skin.
Place patch around eye and leave on for 1 hour then remove.

IONTOPHORESIS  ANTI AGING SOLUTION I
allantoin lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51985-010
Route of AdministrationCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (ALLANTOIN) ALLANTOIN0.1 mL  in 20 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
DIPROPYLENE GLYCOL 
GLYCERIN 
HYALURONATE SODIUM 
PHENOXYETHANOL 
ARGININE 
PHENYL TRIMETHICONE 
METHYLPARABEN 
XANTHAN GUM 
ADENOSINE 
EDETATE DISODIUM 
Packaging
#Item CodePackage Description
1NDC:51985-010-0120 mL in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34704/01/2010
Labeler - ROCKET ELECTRIC CO., LTD. (688236999)
Registrant - ROCKET ELECTRIC CO., LTD. (688236999)
Establishment
NameAddressID/FEIOperations
ROCKET ELECTRIC CO., LTD.688236999manufacture

Revised: 02/2011
 
ROCKET ELECTRIC CO., LTD.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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