Indications and uses
Hand Sanitizer to help reduce bacteria that can potntially cause disease. For use when soap and water are not available. Recommended for repeated use.
Hand Sanitizer
- Manufacturer
- Atlanta Supersource, Inc.
- Effective date
- 2022-12-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:52:04
Label at a glance#
ProductHand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections
Dosage and administration
Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Contacts and useful links#
Label contents#
Full prescribing information#
Hand Sanitizer Foam BAC
Product Description: Non-Flammable, Non-Toxic Hand Sanitizer for everyday use. Will not dry hands. Reduces Common Harmful Germs and Bacteris. FDA approved formulation, manufactured in an FDA Registered Facility. For use when soap and water is not always available.
NDC: 75056-006-01
Atlanta Supersource, Inc.
3655 Kennesaw 75 Parkway
Suite 100
Kennesaw, Georgia 30144
EMERGENCY RESPONSE PROVIDED BY: Chemtrec 1.800.424.9300
Item Number: CLE219
Proudly Made in the USA
Manufactured in an FDA Registered Facility
Active Ingredient (s)
Benzalkonium Chloride 0.1%
Purpose
Antimicrobial
Uses
Hand Sanitizer to help reduce bacteria that can potntially cause disease. For use when soap and water are not available. Recommended for repeated use.
Warnings
For external use only.
When using this product
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thouroughly with water.
Stop use and ask doctor
if irritation or rash occurs.
Keep out of reach of children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Inactive Ingredients
Water, Laurtrimonium Chloride, Cetrimonium Chloride, Dihydroxyethyl Cocamine Oxide
Glycereth-17 Cocoate, Citric Acid Monohydrate - these are not on the Product Data Sheet and Katie explained they do not need to be listed.
Questions or Comments?
Call us at 833.423.0006
Supersource Instant Hand Sanitizer Rinse-Free Foam
Net Contents: 1 Gallon (3.78L)
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 75056-006-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-5eb3-111a-e063-dadaa90a10e2 | SS Hand Sanitizer Foam - BAC |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75056-006-01 | Hand Sanitizer | 3785 g in 1 BOTTLE, PLASTIC | AEROSOL, FOAM | 3785 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- Hand Sanitizer Foam BAC
- DIHYDROXYETHYL COCAMINE OXIDE
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- CETRIMONIUM CHLORIDE
- WATER
- LAURTRIMONIUM CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75056-006 | 75056-006-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIHYDROXYETHYL COCAMINE OXIDE | 8AR51R3BL5 | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| CETRIMONIUM CHLORIDE | UC9PE95IBP | IACT |
| WATER | 059QF0KO0R | IACT |
| LAURTRIMONIUM CHLORIDE | A81MSI0FIC | IACT |
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 |
|---|---|---|---|---|---|---|
| ef199777-e52d-f9e7-e053-2995a90a76ed | aaa831ca-c231-5a47-e053-2a95a90ab862 | 2022-12-05 | Warnings | ef199777-e52d-f9e7-e053-2995a90a76ed aaa831ca-c231-5a47-e053-2a95a90ab862 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.