Micropoint for Blemishes by Small Lab Co., Ltd.

Micropoint for Blemishes by

Drug Labeling and Warnings

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

Drug Details [pdf]

MICROPOINT FOR BLEMISHES- salicylic acid patch 
Small Lab Co., Ltd.

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.

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salicylic acid

Trehalose
Propanediol
Glycerin
Butylene Glycol
Caprylyl Glycol
Madecassoside
1,2-Hexanediol
Ethylhexylglycerin

acne patch

Keep out of reach of the children

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 15~30 seconds

4. Leave in place for 6 hours (Use it during the day or night)

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

for external use only

MICROPOINT FOR BLEMISHES 
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71184-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.5 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71184-0003-2	6 in 1 PACKAGE	07/30/2020	09/06/2023
1	NDC: 71184-0003-1	3 mg in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/30/2020	09/06/2023

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(71184-0003)

Revised: 9/2023

Document Id: 04ab733f-76e9-24b4-e063-6294a90a1d6c

34390-5

Set id: aba11f3d-067f-66f9-e053-2a95a90a26db

Version: 2

Effective Time: 20230906