Dosage and administration
Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Continue to rub hands until dry.
Sanitizer Station Hand Sanitizer Foam
- Manufacturer
- Pharmore Group LLC DBA Sanitizer Station
- Effective date
- 2021-01-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:41:17
Label at a glance#
ProductSanitizer Station Hand Sanitizer Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections
Contacts and useful links#
Websitewww.sanitizer-station.net
www.sanitizer-station.net
www.sanitizer-station.netLabel contents#
Full prescribing information#
Active Ingredient[s]
Benzalkonium Chloride 0.13%
Purpose
Antimicrobial
Use[s]
Hand sanitizer to help reduce bacteria that potentially can cause disease.
For use when soap and water are not available.
Warnings
For external use only.
Do not use
• in children less than 2 months of age
• on open skin wounds
When using this product avoid contact with eyes.
In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask doctor if irritation or redness develops, or if condition persists for more than 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Pump a small amount of foam into palm of hand.
- Rub thoroughly over all surfaces of both hands.
- Continue to rub hands until dry.
Inactive Ingredients
deionized water, glycerin, aloe barbadensis leaf juice, lauramine oxide, dimethyltetradecylamine oxide, fragrance, DMDM hydantoin (preservative).
SPL UNCLASSIFIED SECTION
- Non-Alcoholic Formulation
- Kills viruses, germs and bacteria
- Fragranced
Manufactured by Shotwell Hydrogenics LLC, 10001
West l-20, Suite F-3 Midland, TX 70760
Distributed by Sanitizer Station, 101 Industrial Ct, Conroe, TX, 77301
Packaging
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 82062-201-50 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a309-d8a0-e053-dadaa90a6e4e | Sanitizer Station Hand Sanitizer Foam |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82062-201-50 | Sanitizer Station Hand Sanitizer Foam | 3785 mL in 1 CONTAINER | SOLUTION | 3785 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Sanitizer Station Hand Sanitizer Foam
- Benzalkonium Chloride
- BENZALKONIUM
- WATER
- GLYCERIN
- ALOE VERA LEAF
- LAURAMINE OXIDE
- MYRISTAMINE OXIDE
- DMDM HYDANTOIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82062-201 | 82062-201-50 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| LAURAMINE OXIDE | 4F6FC4MI8W | IACT |
| MYRISTAMINE OXIDE | J086PM3RRT | IACT |
| DMDM HYDANTOIN | BYR0546TOW | 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 |
|---|---|---|---|---|---|---|
| 2d8c6476-7a96-48f9-bf38-530ec7647e74 | 6dfd9bcd-7f0e-477a-9617-ab32fcf4ac64 | 2021-01-07 | Warnings | 2d8c6476-7a96-48f9-bf38-530ec7647e74 6dfd9bcd-7f0e-477a-9617-ab32fcf4ac64 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.