Storage and handling
Other information store in a cool, dry place below 104 o F (40 o C)
SANMAXX Hand Sanitizer Foam
- Manufacturer
- G&N Enterprise,LLC
- Effective date
- 2020-06-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:25:57
Label at a glance#
ProductSANMAXX Hand Sanitizer Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Benzalkonium Chloride 0.13%
OTC - PURPOSE SECTION
Purpose
Antiseptic
INDICATIONS & USAGE SECTION
Uses
- handwash to help reduce bacteria that potentially can cause disease
- helps to prevent cross-contamination by hand contact
- helps to prevent drying of the skin
- recommended for repeated use
WARNINGS SECTION
Warnings
For external use only
OTC - WHEN USING SECTION
When using this product do not use in or near eyes
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or redness develop.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
If swallowed, seek medical attention or contact a Poison Control Center immediately.
DOSAGE & ADMINISTRATION SECTION
Directions
- apply appropriate amount of product into palm of hand
- rub thouroughtly over all surfaces of both hands for at least 20 seconds
- rub hands together until dry
STORAGE AND HANDLING SECTION
Other information
store in a cool, dry place below 104
o F (40
o C)
INACTIVE INGREDIENT SECTION
Inactive ingredients
Water, cocamidopropyl betaine, glycerine, polozamer 124, benzyl alcohol, phenoxyethanol,dehydroacetic acid, sodium hydroxide, citric acid,FD&C Blue No.1
OTC - QUESTIONS SECTION
Questions?
Contact G&N Enterprise, LLC at
800-290-6816 Mon-Fri 9 am-5 pm CST
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
SAN MAXX
Hand Sanitizer
Non_Alcohol
Microbiological Shield
Benzalkonium Chloride 0.13%
Products#
Every source-derived product name is available through these pages.
- SANMAXX Hand Sanitizer Foam
- BENZALKONIUM CHLORIDE
- WATER
- COCAMIDOPROPYL BETAINE
- GLYCERIN
- POLOXAMER 124
- BENZYL ALCOHOL
- PHENOXYETHANOL
- FD&C BLUE NO. 1
- DEHYDROACETIC ACID
- SODIUM HYDROXIDE
- CITRIC ACID MONOHYDRATE
- BENZALKONIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69731-040 | 69731-040-01, 69731-040-02, 69731-040-03, 69731-040-05, 69731-040-08, 69731-040-10, 69731-040-09 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| COCAMIDOPROPYL BETAINE | 5OCF3O11KX | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| POLOXAMER 124 | 1S66E28KXA | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| DEHYDROACETIC ACID | 2KAG279R6R | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
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 |
|---|---|---|---|---|---|---|
| b789aadc-ce14-5913-e053-2995a90a7222 | a7fa2e75-50d7-0746-e053-2a95a90aa86f | 2020-12-28 | Warnings | a7fa2e75-50d7-0746-e053-2a95a90aa86f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.