AC Control Serum

Manufacturer
MIGUHARA
Effective date
2016-02-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:45:03

Label at a glance#

ProductAC Control Serum
Active ingredientAllantoin
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Allantoin 0.2%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Lavandula angustifolia (Lavender) flower extract, Alcohol, Lavandula angustifolia (Lavender) extract, Rosmarinus officinalis (Rosemary) extract, Thymus vulgaris (Thyme) extract, Mentha arvensis leaf extract, Borago officinalis extract, Salvia officinalis (Sage) leaf extract, Jasminum officinale (Jasmine) extract, Anthemis nobilis flower extract, Eclipta prostrata extract, Rehmannia glutinosa root extract, Artemisia princeps leaf extract, Portulaca oleracea extract, Glycyrrhiza glabra (Licorice) root extract, Butylene glycol, Sodium hyaluronate, Lonicera japonica(Honeysuckle) flower extract, Zanthoxylum piperitum fruit extract, Pulsatilla koreana extract, Citrus paradisi(Grapefruit) fruit extract, Citrus aurantium dulcis(Orange) fruit extract, Citrus medica limonum(Lemon) fruit extract, Pyrus malus(Apple) fruit extract, Dimethyl sulfone, Glycosyl trehalose, Hydrogenated starch hydrolysate, Arginine, Carbomer, PEG-60 hydrogenated castor oil, Menthol, Disodium EDTA, Rosmarinus officinalis (Rosemary) leaf oil

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings:

1. Stop usage immediately if any of the below symptoms occur. Continued use could aggravate symptoms, so it is advisable to consult with a dermatologist immediately. 1) Symptoms include but not limited to: red spots, swelling, itchiness. 2) When having the same symptoms as above due to direct sunlight. 2. Do not apply to areas affected by dermatitis, eczema or wounds. 3. Storage and handling: 1) Tightly close lid after each use. 2 Keep out of reach of children 3) Store in a cool dry area, away from sunlight

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Usage

INDICATIONS & USAGE SECTION

Usage: An appropriate amount and evenly apply it on the face along the skin texture.

Usage

DOSAGE & ADMINISTRATION SECTION

Usage: An appropriate amount and evenly apply it on the face along the skin texture.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70380-070-012020-01-31C16284748780-19d75b9d0-4ad7-f424-e053-dadaa90a57ce7bd6ae6a-5414-4595-a986-7dfccfd01572

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70380-070-01AC Control Serum50 mL in 1 CARTONCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70380-070AC CONTROL SERUM (ALLANTOIN) CREAM [MIGUHARA]1Legacy NDC, 1 package rows20160218_7bd6ae6a-5414-4595-a986-7dfccfd01572.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70380-07070380-070-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

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
7898579a-57a4-45d2-9a52-127cd6a4f4877bd6ae6a-5414-4595-a986-7dfccfd015722016-02-18WarningsExact identifier
spl id: 7898579a-57a4-45d2-9a52-127cd6a4f487
spl set id: 7bd6ae6a-5414-4595-a986-7dfccfd01572

Reported adverse events (FAERS/openFDA)#

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