PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER CUCUMBER MELON- alcohol gel PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER ORIGINAL SCENT- alcohol gel PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER SWEET PEACH- alcohol gel PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER SWEET PEA- alcohol gel

PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER SWEET PEA by

Drug Labeling and Warnings

PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER SWEET PEA by is a Otc medication manufactured, distributed, or labeled by American Consumer Products Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient: Ethyl Alcohol 62%

Purpose

Purpose: Antimicrobial

Warnings

Warnings - For external use only. Flammable. Keep away from fire or flame.

Stop Use

Stop use and ask a doctor if: irritation and redness Develops and lasts more than 72 hours.

Keep out of reach of children

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

Directions

Directions - Place enough product in palm to thoroughly cover your hands. Rub hands together briskly undtil dry. Children under 6 years of age should be supervised when using this product. Other information: *Store below 110o F (43o C) May discolor certain fabrics or surfaces.

Inactive Ingredients

Inactive Ingredients: Water, Aloe Barbadensis Gel, Carbomer, Fragrance, Glycerin, Triethanolamine, Tocopheryl Acetate.

Indications & Usage Section

When using this product: do not use in or near the eyes. In case of eye contact, flush eyes thoroughly with water.

Pharmacy's Prescription 1.8 OZ Labels

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER CUCUMBER MELON 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER 980 (UNII: 4Q93RCW27E)
ALOE ARBORESCENS WHOLE (UNII: 0EF00WD7LU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-005-01	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/31/2018

PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER ORIGINAL SCENT 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
ALOE ARBORESCENS WHOLE (UNII: 0EF00WD7LU)
WATER (UNII: 059QF0KO0R)
CARBOMER 980 (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-003-01	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/31/2018

PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER SWEET PEACH 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
ALOE ARBORESCENS WHOLE (UNII: 0EF00WD7LU)
WATER (UNII: 059QF0KO0R)
CARBOMER 980 (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-004-01	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/31/2018

PHARMACYS PRESCRIPTION 1.8OZ HAND SANITIZER SWEET PEA 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER 980 (UNII: 4Q93RCW27E)
ALOE ARBORESCENS WHOLE (UNII: 0EF00WD7LU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-006-01	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/31/2018

Labeler - American Consumer Products Corp (081101181)