IM FILL- hyaluronic acid patch

Im Fill by

Drug Labeling and Warnings

Im Fill by is a Otc medication manufactured, distributed, or labeled by Karatica Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium Hyaluronate

INACTIVE INGREDIENT

Acetyl Hexapeptide-8

PURPOSE

Multi Function - Anti-Wrinkle Moisturizing

KEEP OUT OF REACH OF CHILDREN

keep out or reach of the children

INDICATIONS & USAGE

1) Apply toner or emulsion to cleansed face.

2) Open the pouch and take the patches out from the plastic case carefully.

(Be careful not to touch the center area with fingers.)

3) Remove the white films on the patches and attach it on the desired area.

4) Remove the transparent films and press vertically the patches on the skin several times with your fingers.

5) Remove the patches after 2 hours (or next morning) and clean the face.

*2 or 3 day interval or 2 times per week is recommended for regular use.

WARNINGS

1) Discontinue use or consult dermatologist if irritation, itching or swelling appears after applying the product.

2) Avoid applying patches on the wounded, inflamed or other uncomfortable skin part.

3) Cautions for the storage and handling a) Keep out of children. B) Avoid hot or cold and direct sunlight. c) After unpacking, use the patches immediately to prevent deterioration.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IM FILL 
hyaluronic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70514-0009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONATE SODIUM	99.97 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70514-0009-1	4 in 1 PACKAGE	11/29/2017
1		0.8 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/29/2017

Labeler - Karatica Co., Ltd (689605545)

Registrant - Karatica Co., Ltd (689605545)

Establishment
Name	Address	ID/FEI	Business Operations
Karatica Co., Ltd		689605545	manufacture(70514-0009)