Mighty Patch Micropoint for Blemishes,Salicylic Acid 0.5% Acne Treatment

Manufacturer
Hero Cosmetics, Inc.
Effective date
2019-10-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:03:39

Label at a glance#

ProductMighty Micropoint for Blemishes,Salicylic Acid 0.5 Acne Treatment
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

• For the treatment of acne

Dosage and administration

• Clean the skin before applying this product. Apply the patch and press down for 15-30 seconds. Remove after 6 hours. Use 1-2 patches for best results.v

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.5%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

• For the treatment of acne

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• Clean the skin before applying this product. Apply the patch and press down for 15-30 seconds. Remove after 6 hours. Use 1-2 patches for best results.v

Other information

SPL UNCLASSIFIED SECTION

Store at 34°F-86°F (1°C-30°C)for best results

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beta glucan, butylene glycol, caprylyl glycol, dipotassium glycyrrhizate, ethoxydiglycol, ethylhexylglycerin, glycerin, 1,2-hexanediol, madecassoside, propanediol, sodium hyaluronate, tea tree leaf oil, totarol, trehalose

Questions or Comments?

OTC - QUESTIONS SECTION

347-669-0686

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73381-00073381-000-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e3268df4-053b-1fd4-e053-2a95a90ace1e4c9ec3a7-66d2-4d21-a0fb-ef816560b8c82022-07-06WarningsExact identifier
spl set id: 4c9ec3a7-66d2-4d21-a0fb-ef816560b8c8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.