MY BEAUTY SPOT Day and Night Acne Patch

Manufacturer
MELON BIO-TECH (THAILAND) CO., LTD.
Effective date
2025-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:59:57

Label at a glance#

ProductMY BEAUTY SPOT Day and Night Acne Patch
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

soothe and help diminish the redness and irritation of blemished skin and asorbs excess oil for faster healing.

Dosage and administration

Cleanse and dry facem, removing any makeup. Apply one healing dot, sticky side down, over your blemish. Leave the healing dot over blemish for at least 6 hours or overnight Repeat as necessary with a new healing dot.

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

soothe and help diminish the redness and irritation of blemished skin and asorbs excess oil for faster healing.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Cleanse and dry facem, removing any makeup.
  • Apply one healing dot, sticky side down, over your blemish.
  • Leave the healing dot over blemish for at least 6 hours or overnight
  • Repeat as necessary with a new healing dot.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Calcium Carboxymethyl Cellulose, Polysilicone-2, Butylene Glycol. Polyurethane-42, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Sodium Hyaluronate. May contain: FD&C Red No. 40 (CI 16035), FD&C Red No.4 (CI 14700), FD&C Yellow No.5 (CI 19140), FD&C Blue No.1 (CI 42090).

Warnings

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control center right away

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1994404salicylic acid 0.5 % Medicated PatchPSN1
1994404salicylic acid 0.005 MG/MG Medicated PatchSCD1
1994404salicylic acid 0.5 % Medicated PatchSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85588-101-01MY BEAUTY SPOT Day and Night Acne Patch0.051 g in 1 PATCHPATCH0.0511
85588-101-01MY BEAUTY SPOT Day and Night Acne Patch40 in 1 PACKAGEPATCH401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85588-101MY BEAUTY SPOT DAY AND NIGHT ACNE PATCH (SALICYLIC ACID) PATCH [MELON BIO-TECH (THAILAND) CO., LTD.]1Current NDC, 2 package rows20250430_6e4ab3d3-378e-40e5-a6a5-66090edcfda8.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85588-10185588-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
MY BEAUTY SPOT Day and Night Acne PatchSALICYLIC ACIDMELON BIO-TECH (THAILAND) CO., LTD.6e4ab3d3-378e-40e5-a6a5-66090edcfda82025-04-28WarningsExact identifier
ndc (package): 85588-101-01
ndc (product): 85588-101
ndc11 (package): 85588010101
spl id: 33e2836f-e404-afb8-e063-6394a90a454e
spl set id: 6e4ab3d3-378e-40e5-a6a5-66090edcfda8

Reported adverse events (FAERS/openFDA)#

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