HANHOO BlemishPatch

Manufacturer
New Bio Pharmaceutical Co., Ltd.
Effective date
2023-12-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:03:36

Label at a glance#

ProductHANHOO BlemishPatch
Active ingredientMINERAL OIL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

mineral oil

OTC - PURPOSE SECTION

skin protectant

for the treatment of acne

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

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 15~30 seconds

4. Leave in place for 6 hours (Use it during the day or night)

WARNINGS SECTION

For external use only

When using this product

■ if following abnormal symptoms persist, discontinue use

Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes

■ Stop immediately and consult a doctor if you experience

1) Hypersensitivity symptoms such as erythema, itching and dermatitis.

2) Skin Irritation

3) Following Instructions when using medication

(1) For external use only (Do not use internally)

(2) Avoid getting into the eyes (if contact occurs, wash well with clean water)

INACTIVE INGREDIENT SECTION

water

DOSAGE & ADMINISTRATION SECTION

For topical use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83857-0001-1HANHOO BlemishPatch5 g in 1 PACKAGEPATCH51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83857-0001HANHOO BLEMISHPATCH (MINERAL OIL) PATCH [NEW BIO PHARMACEUTICAL CO., LTD.]11 package rows20231208_0bf2ffa3-c87f-1297-e063-6394a90ab057.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83857-000183857-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
MINERAL OILT5L8T28FGPACTIB
WATER059QF0KO0RIACT

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
0bf2f33a-af99-30a8-e063-6294a90a93490bf2ffa3-c87f-1297-e063-6394a90ab0572023-12-07WarningsExact identifier
spl id: 0bf2f33a-af99-30a8-e063-6294a90a9349
spl set id: 0bf2ffa3-c87f-1297-e063-6394a90ab057

Reported adverse events (FAERS/openFDA)#

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