SANMAXX Hand Sanitizer Foam by G&N Enterprise,LLC SAN MAXX Hand Sanitizer

SANMAXX Hand Sanitizer Foam by

Drug Labeling and Warnings

SANMAXX Hand Sanitizer Foam by is a Otc medication manufactured, distributed, or labeled by G&N Enterprise,LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SANMAXX HAND SANITIZER FOAM- benzalkonium chloride liquid 
G&N Enterprise,LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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SAN MAXX Hand Sanitizer

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

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

For external use only

When using this product do not use in or near eyes

Stop use and ask a doctor if irritation or redness develop.

Keep out of reach of children.

If swallowed, seek medical attention or contact a Poison Control Center immediately.

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

Other information

store in a cool, dry place below 104 o F (40 o C)

Inactive ingredients

Water, cocamidopropyl betaine, glycerine, polozamer 124, benzyl alcohol, phenoxyethanol,dehydroacetic acid, sodium hydroxide, citric acid,FD&C Blue No.1

Questions?

Contact G&N Enterprise, LLC at 800-290-6816 Mon-Fri 9 am-5 pm CST

SAN MAXX

Hand Sanitizer

Non_Alcohol

Microbiological Shield

Benzalkonium Chloride 0.13%

SANMAXX HAND SANITIZER FOAM 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69731-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
POLOXAMER 124 (UNII: 1S66E28KXA)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69731-040-01	946352 mL in 1 TANK; Type 0: Not a Combination Product	05/01/2020	12/28/2020
2	NDC: 69731-040-02	208197 mL in 1 DRUM; Type 0: Not a Combination Product	05/01/2020	12/28/2020
3	NDC: 69731-040-03	3785 mL in 1 JUG; Type 0: Not a Combination Product	05/01/2020	12/28/2020
4	NDC: 69731-040-05	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020	12/28/2020
5	NDC: 69731-040-08	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020	12/28/2020
6	NDC: 69731-040-10	45 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020	12/28/2020
7	NDC: 69731-040-09	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020	12/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2020	12/28/2020

Labeler - G&N Enterprise,LLC (079758164)

Revised: 12/2020

Document Id: b789aadc-ce14-5913-e053-2995a90a7222

34390-5

Set id: a7fa2e75-50d7-0746-e053-2a95a90aa86f

Version: 2

Effective Time: 20201228