IONTOPHORESIS ANTI AGING SOLUTION I- allantoin lotion

IONTOPHORESIS by

Drug Labeling and Warnings

IONTOPHORESIS by is a Otc medication manufactured, distributed, or labeled by ROCKET ELECTRIC CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Allantoin

INACTIVE INGREDIENT

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

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

WARNINGS

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

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

INDICATIONS & USAGE

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 & ADMINISTRATION

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IONTOPHORESIS  ANTI AGING SOLUTION I
allantoin lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51985-010
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.1 mL  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ARGININE (UNII: 94ZLA3W45F)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
METHYLPARABEN (UNII: A2I8C7HI9T)
XANTHAN GUM (UNII: TTV12P4NEE)
ADENOSINE (UNII: K72T3FS567)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51985-010-01	20 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	04/01/2010

Labeler - ROCKET ELECTRIC CO., LTD. (688236999)

Registrant - ROCKET ELECTRIC CO., LTD. (688236999)

Establishment
Name	Address	ID/FEI	Business Operations
ROCKET ELECTRIC CO., LTD.		688236999	manufacture