FDA.reportPublic FDA data

scar gel

Manufacturer
Guangzhou Meayon Biotechnology Co,.Ltd
Effective date
2022-08-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:50:31

Label at a glance#

Productscar gel
Active ingredientALLANTOIN
Label structure12 sections

Dosage and administration

condition worsens symptoms last more than 7daysor clear up and occur again within a few days DO not use on.

Storage and handling

/

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.3%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Use

INDICATIONS & USAGE SECTION

Temporarily protects and helps relieve chapped or cracked skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

do not get into eyes.

OTC - STOP USE SECTION

condition worsens symptoms last more than 7daysor clear up and occur again within a few days DO not use on.
deep or puncture wounds animal bites serious burns.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

condition worsens symptoms last more than 7daysor clear up and occur again within a few days DO not use on.

Other information

STORAGE AND HANDLING SECTION

/

Inactive ingredients

INACTIVE INGREDIENT SECTION

CYCLOPENTASILOXANE
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER

HEXYLDECANOL
STEARIC ACID
BRASSICA CAMPESTRIS (RAPESEED) STEROLS
ARGANIA SPINOSA KERNEL OIL
TOCOPHERYL ACETATE
CERAMIDE 3
CERAMIDE 6 II
CHOLESTEROL
MADECASSOSIDE

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75728-004-01 15 g in 1 BOTTLE

75728-004-01 15 g in 1 BOTTLE75728-004-01 15 g in 1 BOTTLE

75728-004-02 20 g in 1 BOTTLE

75728-004-02 20 g in 1 BOTTLE75728-004-02 20 g in 1 BOTTLE

75728-004-03 30 g in 1 BOTTLE

75728-004-03 30 g in 1 BOTTLE75728-004-03 30 g in 1 BOTTLE

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75728-004-012023-07-28C16284748780-10191ceaa-63d9-198a-e063-dbdaa90aec3e75728-004 scar gel
75728-004-022023-07-28C16284748780-10191ceaa-63d9-198a-e063-dbdaa90aec3e75728-004 scar gel
75728-004-032023-07-28C16284748780-10191ceaa-63d9-198a-e063-dbdaa90aec3e75728-004 scar gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75728-004-01scar gel15 g in 1 BOTTLEGEL153
75728-004-02scar gel20 g in 1 BOTTLEGEL203
75728-004-03scar gel30 g in 1 BOTTLEGEL303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75728-004SCAR GEL (SCAR CREAM) GEL [GUANGZHOU MEAYON BIOTECHNOLOGY CO,.LTD]3Legacy NDC, 3 package rows20220825_bea7e59b-ac34-3955-e053-2995a90a5cd5.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75728-00475728-004-01, 75728-004-03, 75728-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
HEXYLDECANOL151Z7P1317IACT
STEARIC ACID4ELV7Z65APIACT
ALLANTOIN344S277G0ZACTIB
RAPESEED STEROLB46B6DD20UIACT
ARGAN OIL4V59G5UW9XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CERAMIDE 34370DF050BIACT
CERAMIDE 6 IIF1X8L2B00JIACT
CHOLESTEROL97C5T2UQ7JIACT
MADECASSOSIDECQ2F5O6YIYIACT
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT

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
e6f87686-6229-5f8d-e053-2a95a90ab99fbea7e59b-ac34-3955-e053-2995a90a5cd52022-08-24WarningsExact identifier
spl id: e6f87686-6229-5f8d-e053-2a95a90ab99f
spl set id: bea7e59b-ac34-3955-e053-2995a90a5cd5

Reported adverse events (FAERS/openFDA)#

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