SNUGZ BEADED HAND SANITIZER GEL- beaded hand sanitizer gel gel

SnugZ Beaded Hand Sanitizer Gel by

Drug Labeling and Warnings

SnugZ Beaded 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 BEADED HAND SANITIZER GEL 
beaded hand sanitizer gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76309-350
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)
ETHYLHEXYL PALMITATE (UNII: 2865993309)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76309-350-01	28 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
2	NDC: 76309-350-02	56 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
3	NDC: 76309-350-04	112 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
4	NDC: 76309-350-08	224 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2018
5	NDC: 76309-350-19	56 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
6	NDC: 76309-350-51	30 mL in 1 TUBE; Type 0: Not a Combination Product	01/01/2018
7	NDC: 76309-350-61	39.75 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2018
8	NDC: 76309-350-62	85.17 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2018
9	NDC: 76309-350-81	28 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
10	NDC: 76309-350-91	28 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2018
11	NDC: 76309-350-05	14 mL in 1 BOTTLE; 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(76309-350)