M SKIN CARE MICRONEEDLE BLEMISH PATCHES- salicylic acid 0.5% patch
SALES AND PRODUCT SOLUTIONS

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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M Skin Care Microneedle Blemish Patches

Active Ingredient

Salicylic Acid 0.5%

Purpose

Acne Treatment

Use

For the Treatment of Acne
Clears up Acne blemish, blackheads and allows skin to heal

Warnings

For external use only.

When using this product

Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Before applying patches, thoroughly cleanse and dry the affected area
Apply patch and press down for 15 seconds, patting the edges of patch to secure and contain the blemish.
Leave the patch in place for at least 6 hours or overnight to permit healing
To remove, gently peel back and discard
Cleanse affected area and repeat application with a fresh blemish patch, if desired.

Inactive Ingredients

Sodium Hyaluronate, Trehalose, Propanediol, Caprylyl Glycol, Madecassoside, Dipotassium Glycyrrhizate, Ethylhexylglycerin

M Skin Care Microneedle Blemish Patches

label

M SKIN CARE MICRONEEDLE BLEMISH PATCHES
salicylic acid 0.5% patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:37520-007
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
TREHALOSE (UNII: B8WCK70T7I)
PROPANEDIOL (UNII: 5965N8W85T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
MADECASSOSIDE (UNII: CQ2F5O6YIY)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:37520-007-06	1 g in 1 PACKET; Type 0: Not a Combination Product	01/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	01/01/2021

Labeler - SALES AND PRODUCT SOLUTIONS (037519852)

Registrant - SALES AND PRODUCT SOLUTIONS (037519852)

Name	Address	ID/FEI	Business Operations
Establishment
Small Lab Co., Ltd.		688438425	manufacture(37520-007)