HARUTO BEAUTY MICRONEEDLE ACNE PIMPLEPATCH

Manufacturer
Small Lab Co., Ltd.
Effective date
2023-09-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:26:30

Label at a glance#

ProductHARUTO BEAUTY MICRONEEDLE ACNE PIMPLEPATCH
Active ingredientHYALURONATE SODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

SODIUM HYALURONATE

INACTIVE INGREDIENT SECTION

Trehalose
Propanediol
Calendula Officinalis Flower Extract
Panthenol
Glycerin
Butylene Glycol
Caprylyl Glycol
Madecassoside
Salicylic Acid
1,2-Hexanediol
Ethylhexylglycerin

OTC - PURPOSE SECTION

acne patch

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the 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 2-3 minutes.

4. Leave in place for 2 hours or more.(Use it during the day or night)

WARNINGS SECTION

1. Do not use in the following cases(Eczema and scalp wounds)

2.Side Effects

1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor

3.General Precautions

1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately

2)This product is for exeternal use only. Do not use for internal use

4.Storage and handling precautions

1)If possible, avoid direct sunlight and store in cool and area of low humidity

2)In order to maintain the quality of the product and avoid misuse

3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71184-0002-12023-09-06C16284748780-1d6a99b39-a63a-a426-e053-dadaa90af4c2a5d685bb-7141-44c5-e053-2995a90a1d3d
71184-0002-12022-01-28C16284748780-1d6a99b39-a63a-a426-e053-dadaa90af4c2a5d685bb-7141-44c5-e053-2995a90a1d3d

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71184-000271184-0002-1

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
HYALURONATE SODIUMYSE9PPT4THACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

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
04ab4bc8-af70-711c-e063-6294a90ac13ea5d685bb-7141-44c5-e053-2995a90a1d3d2023-09-06WarningsExact identifier
spl id: 04ab4bc8-af70-711c-e063-6294a90ac13e
spl set id: a5d685bb-7141-44c5-e053-2995a90a1d3d

Reported adverse events (FAERS/openFDA)#

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