Dosage and administration
press pump down to dispense liquid hand soap onto moistened hands,lather and rinse thoroughly
antibacterial hand sanitizer
- Manufacturer
- Hangzhou Guoguang Touring Commodity Co., Ltd.
- Effective date
- 2018-01-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 22:54:00
Label at a glance#
Productantibacterial hand sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections
Label contents#
Full prescribing information#
Active Ingredient
Benzalkonium chloride 0.1%
Purpose
Antispetic
Use
for hand washing to decrease bacteria on skin
WARNINGS
For External use only-hands.
Avoid contact with eyes,in case of contact ,flush with water.
Keep out of direct sunlight
do not drink,not edible
keep out of reach of children
keep out of reach of children
Directions
press pump down to dispense liquid hand soap onto moistened hands,lather and rinse thoroughly
Inactive ingredients
aqua ,sodium laureth sulfate,cocamidopropyl betaine,disodium cocoamphodiacetate,cocamide MEDA,Glycerin,Aloe Barbadensis leaf juice,PEG-7 glyceryl cocoate,sodium chloride,citric acid ,disodium EDTA,tocopheryl acetate,methylisothiazolinone,lodopropynyl butylcarbamate
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 61312-007-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-c769-f424-e053-dadaa90a57ce | Hand Soap |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61312-007-01 | antibacterial hand sanitizer | 221 g in 1 BOTTLE | GEL | 221 | 3 | |
| 61312-007-01 | antibacterial hand sanitizer | 24 in 1 CARTON | GEL | 24 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- antibacterial hand sanitizer
- Benzalkonium Chloride
- WATER
- GLYCERIN
- SODIUM LAURETH SULFATE
- SODIUM CHLORIDE
- DISODIUM COCOAMPHODIACETATE
- COCAMIDE
- BENZALKONIUM
- ALOE VERA LEAF
- GLYCERYL COCOATE
- CITRIC ACID ACETATE
- DISODIUM EDTA-COPPER
- TOCOPHERYL RETINOATE
- METHYLISOTHIAZOLINONE
- IODOPROPYNYL BUTYLCARBAMATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 61312-007 | 61312-007-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 621793d7-3fec-5379-e053-2a91aa0a11c8 | 3f7f37f9-ac16-65d3-e054-00144ff8d46c | 2018-01-06 | Warnings | 621793d7-3fec-5379-e053-2a91aa0a11c8 3f7f37f9-ac16-65d3-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.