FDA.reportPublic FDA data

Raw Instant Hand Sanitizer Gel

Manufacturer
Raw Office Inc, The | Guangzhou Gotdya Fine Chemical Co., Ltd.
Effective date
2020-07-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:22:43

Label at a glance#

ProductRaw Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Storage: Keep tightly closed in a cool, dark, dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Main Active ingredient: Alcohol 75% W/W

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Uses

Suitable for hand, skin and object surface sanitization

WARNINGS SECTION

Precautions:

  1. This product is for external use only. Do not take it internally.
  2. Do not use in case of wounds in the treated areas or of alcohol allergy.
  3. This product is flammable. Keep away from sources of ignition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

4. Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Usuage: Put proper amount of the Hand Sanitizer into your palm and gently rub it over your palms, the back of your hands, fingers and the spaces between your fingers. Rub your hands together continuously until they are dry.

STORAGE AND HANDLING SECTION

Storage: Keep tightly closed in a cool, dark, dry place.

INACTIVE INGREDIENT SECTION

Ingredients: Alcohol, Water, Propylene glycol, Carbomer, Aminomethyl Propanol

SPL UNCLASSIFIED SECTION

Kills Germs

Types of Microbes To Be Inhibited:

Can inhibit staphylococcus aureus, Candida albicans and Escherichia coli.

rawoffice.com

MADE IN CHINA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75353-614-502023-07-11C16284748780-1f386c649-ebf4-0266-e053-dadaa90a7c1aRaw Instant Hand Sanitizer Gel
75353-614-502023-01-30C16284748780-1f386c649-ebf4-0266-e053-dadaa90a7c1aRaw Instant Hand Sanitizer Gel

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
75353-61475353-614-50

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
0037626f-73e0-d805-e063-6394a90ae2ee6d4dbe7b-b92e-4096-b34f-a1156eb8c3cd2023-07-11WarningsExact identifier
spl set id: 6d4dbe7b-b92e-4096-b34f-a1156eb8c3cd

Reported adverse events (FAERS/openFDA)#

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