Hand Sanitizer, Gel

Manufacturer
B & J Group
Effective date
2021-12-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:21:03

Label at a glance#

ProductHand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use(s)

INDICATIONS & USAGE SECTION

Hand sanitizer that can help reduce bacteria that can cause disease. Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame. For external use only.

Do not use

OTC - DO NOT USE SECTION

  • In children less than two months of age
  • On open skin wounds

When using this product

OTC - WHEN USING SECTION

do NOT use near eyes, ears or mouth. In case of contact, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Direction

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover your hands. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

SPL UNCLASSIFIED SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing or heat above 40C (104F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

glycerin, carbomer, water, fragrance

Package Labeling:118.3ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box3Box3

Package Labeling:236.6ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box4Box4

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
69737-00369737-003-00, 69737-003-01

Ingredients#

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

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

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
d3d1a54b-5afc-fbc1-e053-2995a90a6237243056d4-1ef8-4346-8920-38cd70a346522021-12-23WarningsExact identifier
spl id: d3d1a54b-5afc-fbc1-e053-2995a90a6237
spl set id: 243056d4-1ef8-4346-8920-38cd70a34652

Reported adverse events (FAERS/openFDA)#

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