ACNEPATCH- sodium hyaluronate patch

ACNEPATCH by

Drug Labeling and Warnings

ACNEPATCH by is a Otc medication manufactured, distributed, or labeled by Small Lab Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

SODIUM HYALURONATE

INACTIVE INGREDIENT

Trehalose
Propanediol
Calendula Officinalis Flower Extract
Panthenol
Glycerin
Butylene Glycol
Caprylyl Glycol
Madecassoside
Salicylic Acid
1,2-Hexanediol
Ethylhexylglycerin

PURPOSE

acne patch

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of the children

INDICATIONS & USAGE

1. After cleansing, keep your skin clearly.

2. Carefully remove dots from the film.

3. Stick the patch to target areas of concern and gently press down on the patch for 2-3 minutes.

4. Leave in place for 2 hours or more.(Use it during the day or night)

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)

2.Side Effects

1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor

3.General Precautions

1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately

2)This product is for exeternal use only. Do not use for internal use

4.Storage and handling precautions

1)If possible, avoid direct sunlight and store in cool and area of low humidity

2)In order to maintain the quality of the product and avoid misuse

3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACNEPATCH 
sodium hyaluronate patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71184-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONATE SODIUM	0.4298 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71184-0001-1	3 mg in 1 PATCH; Type 0: Not a Combination Product	04/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/28/2020

Labeler - Small Lab Co., Ltd. (688438425)

Registrant - Small Lab Co., Ltd. (688438425)

Establishment
Name	Address	ID/FEI	Business Operations
Small Lab Co., Ltd.		688438425	manufacture(71184-0001)