HARUTO BEAUTY MICRONEEDLE ACNE PIMPLEPATCH- sodium hyaluronate 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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SODIUM HYALURONATE

Trehalose
Propanediol
Calendula Officinalis Flower Extract
Panthenol
Glycerin
Butylene Glycol
Caprylyl Glycol
Madecassoside
Salicylic Acid
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 2-3 minutes.

4. Leave in place for 2 hours or more.(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

label

HARUTO BEAUTY MICRONEEDLE ACNE PIMPLEPATCH 
sodium hyaluronate patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71184-0002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.4298 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71184-0002-13 mg in 1 PATCH; Type 0: Not a Combination Product05/17/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/17/2020
Labeler - Small Lab Co., Ltd. (688438425)
Registrant - Small Lab Co., Ltd. (688438425)
Establishment
NameAddressID/FEIBusiness Operations
Small Lab Co., Ltd.688438425manufacture(71184-0002)

Revised: 5/2020
Document Id: a5d685bb-7142-44c5-e053-2995a90a1d3d
Set id: a5d685bb-7141-44c5-e053-2995a90a1d3d
Version: 1
Effective Time: 20200517
 
Small Lab Co., Ltd.