FDA.reportPublic FDA data

Raw antiseptic HAND SANITIZER WIPES

Manufacturer
Raw Office Inc, The
Effective date
2020-11-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:08:36

Label at a glance#

ProductRaw antiseptic HAND SANITIZER WIPES
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on skin

Dosage and administration

Wet hands thoroughly with product and allow to dry.

Storage and handling

■ Store below 43°C (110°F) ■ Keep sealed after use

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% (v/v)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

■ External use, not oral. Keep out of children's reach.

■ Flammable, keep away from fire and flame.

■ Use with caution if allergic to alcohol.

When using this product

Avoid contacting face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask doctor if

■ Irritation or redness occurs.

Keep out of children's reach.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry.

Other Information

STORAGE AND HANDLING SECTION

■ Store below 43°C (110°F)

■ Keep sealed after use

INACTIVE INGREDIENT SECTION

Inactive Ingredients Purified Water, Glycerol, Aloe Vera

SPL UNCLASSIFIED SECTION

Product Use:

Hold and grasp the barrel with both hands then turn the lid counter-clockwise. Take out the wet towel bag, tear the package parallel from the tear hole, pull towel through the centre hole of the barrel lid. Make sure to close lid between uses.

MADE IN CHINA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

PackagingPackaging

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75353-001-012023-07-11C16284748780-1e4f33bdf-9be2-d8a0-e053-dadaa90a6e4eRaw antiseptic HAND SANITIZER wipes
75353-001-022023-07-11C16284748780-1e4f33bdf-9be2-d8a0-e053-dadaa90a6e4eRaw antiseptic HAND SANITIZER wipes
75353-001-012022-07-29C16284748780-1e4f33bdf-9be2-d8a0-e053-dadaa90a6e4eRaw antiseptic HAND SANITIZER wipes
75353-001-022022-07-29C16284748780-1e4f33bdf-9be2-d8a0-e053-dadaa90a6e4eRaw antiseptic HAND SANITIZER wipes

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
75353-00175353-001-01, 75353-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
ffab1941-87d3-a9e7-e053-6294a90a11d004f79a87-da87-4f70-892d-2ad7a08070fa2023-07-04WarningsExact identifier
spl set id: 04f79a87-da87-4f70-892d-2ad7a08070fa

Reported adverse events (FAERS/openFDA)#

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