ACROPASS ACNE CURE - RAPHAS CO., LTD | RAPHAS CO.,LTD

Manufacturer
RAPHAS CO., LTD | RAPHAS CO.,LTD
Effective date
2026-09-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-09-25 02:01:35

Label at a glance#

ProductACROPASS ACNE CURE
Active ingredientSALICYLIC ACID
Label structure13 sections

Storage and handling

Store at room temperature. Avoid use if you have very sensitive skin or anr allergic to Salicylic acid.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Salicylic Acid 2%.................................................... Acne Treatment labellabel

OTC - PURPOSE SECTION

Uses: For the treatment of acnes

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

  • Skin irritation and dryness may occur if you use another topical acne medication at the same time or immediately following.
  • If irritation occurs, only use one topical acne medication at a time unless directed by doctor.

OTC - STOP USE SECTION

if irritation becomes severe.

OTC - ASK DOCTOR SECTION

if irritation becomes severe.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

STORAGE AND HANDLING SECTION

Store at room temperature. Avoid use if you have very sensitive skin or anr allergic to Salicylic acid.

INACTIVE INGREDIENT SECTION

Sodium Hyaluronate, Niacinamide, Oligopeptide-10, Phytosphingosine HCl

Patch : Hydrocolloid

REFERENCES SECTION

labellabel

DOSAGE & ADMINISTRATION SECTION

1. Open the packaging and take out the patch.
2. Carefully remove the white film, ensuring not to touch the center of the patch.
3. Apply the patch directly to the affected area and press vertically with your fingers.
4. Leave on for 2 hours or overnight, then remove.

INDICATIONS & USAGE SECTION

1. Open the packaging and take out the patch.
2. Carefully remove the white film, ensuring not to touch the center of the patch.
3. Apply the patch directly to the affected area and press vertically with your fingers.
4. Leave on for 2 hours or overnight, then remove.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

panelpanel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71134-24171134-241-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-08-26full-release2026-06-01 00:17:53

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
2090f57d-a934-54e3-e063-6394a90ae4441e951033-5de7-e3b3-e063-6394a90a7a5b2024-08-26WarningsExact identifier
spl set id: 1e951033-5de7-e3b3-e063-6394a90a7a5b

Reported adverse events (FAERS/openFDA)#

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