SNUGZ HAND SANITIZER GEL- hand sanitizer gel gel

SnugZ Hand Sanitizer Gel by

Drug Labeling and Warnings

SnugZ Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by SnugZ/USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Wet hands thoroughly with product and rub into skin until dry.

WARNINGS

Warnings: For external use only. Flammable, keep away from fire. Do not use on damaged or broken skin. Keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Inactive Ingredients: Aminomethyl Propanol, Carbomer, Water

ACTIVE INGREDIENT

Active Ingredients: Ethyl Alcohol 63.5%

PURPOSE

Purpose: Antiseptic

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

INDICATIONS & USAGE

Indications: Helps reduce bacteria on skin.

Hand Sanitizer Gel

INGREDIENTS AND APPEARANCE

SNUGZ HAND SANITIZER GEL 
hand sanitizer gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76309-300
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	17.78 mL  in 28 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76309-300-01	28 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
2	NDC: 76309-300-02	56 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
3	NDC: 76309-300-04	112 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
4	NDC: 76309-300-08	224 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2018
5	NDC: 76309-300-19	56 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
6	NDC: 76309-300-51	30 mL in 1 TUBE; Type 0: Not a Combination Product	01/01/2018
7	NDC: 76309-300-05	14 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
8	NDC: 76309-300-81	28 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
9	NDC: 76309-300-91	28 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
10	NDC: 76309-300-61	39.75 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2018
11	NDC: 76309-300-62	85.17 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2018

Labeler - SnugZ/USA, LLC (615959228)

Establishment
Name	Address	ID/FEI	Business Operations
SnugZ/USA, LLC		615959228	manufacture(76309-300)