ANTI-BACTERIAL HAND GEL SWEET PEA- ethyl alcohol gel

Anti-Bacterial Hand Gel Sweet Pea by

Drug Labeling and Warnings

Anti-Bacterial Hand Gel Sweet Pea by is a Otc medication manufactured, distributed, or labeled by The Man Can, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Alcohol 60%

PURPOSE

Purpose
Antiseptic

INDICATIONS & USAGE

Use: Decreases bacteria on hands.

WARNINGS

Warning: For external use only. Flammable.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. 

DOSAGE & ADMINISTRATION

Directions: Rub a dime sized drop into hands                                                                                                                                                          

PRINCIPAL DISPLAY PANEL

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:
Water, Aloe Barbadensis Leaf Juice, Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance, Tocopheryl Acetate, Lactose, Microcrystalline Cellulose, FD&C Red NO.4

INGREDIENTS AND APPEARANCE

ANTI-BACTERIAL HAND GEL SWEET PEA 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59045-1004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
ALOE (UNII: V5VD430YW9)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
LACTOSE (UNII: J2B2A4N98G)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59045-1004-1	29 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/10/2013

Labeler - The Man Can, LLC (063578571)