PUMIN HANDS MUST BE CLEAN- alcohol gel

PUMIN HANDS MUST BE CLEAN by

Drug Labeling and Warnings

PUMIN HANDS MUST BE CLEAN by is a Otc medication manufactured, distributed, or labeled by BRANDHAUS, BRANDHAU. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

alcohol

INACTIVE INGREDIENT

Water
Carbomer
Triethanolamine
Menthol
Aloe Barbadensis Leaf Extract

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

PURPOSE

hand sanitizer to help reduce bacteria that potentially can cause disease

for use when soap and water are not available

INDICATIONS & USAGE

Place enough product on hands to cover all surfaces.Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

WARNINGS

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PUMIN HANDS MUST BE CLEAN 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77601-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER 940 (UNII: 4Q93RCW27E)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77601-0002-1	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/17/2020

Labeler - BRANDHAUS (695695904)

Registrant - BRANDHAUS (695695904)

Establishment
Name	Address	ID/FEI	Business Operations
BRANDHAU		695695904	manufacture(77601-0002) , label(77601-0002)