LA BODIES PURITA ANTI-BACTERIAL HAND SANITIZER- alcohol gel

LA Bodies Purita Anti-Bacterial Hand Sanitizer by

Drug Labeling and Warnings

LA Bodies Purita Anti-Bacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SAMSON PHARMACEUTICAL. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

Ethyl Alcohol 62%

Purpose

Antimicrobial

Inactive Ingredients

Water (Aqua), Propylene Glycol, Aloe Barbadensis Leaf Juice, Glycerin, Tocopheryl Acetate, Carbomer, Triethanolamine, Fragrance (Parfum)

Use

Hand Sanitizer to help reduce bacteria on the skin

Warnings

• Flammable. Keep away from fire or flame. For external use only.
• When using this product do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.
• Stop use and ask doctor if irritation or rash appears and lasts.

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

Directions

Place product on hands. Rub until dry.

SPL UNCLASSIFIED SECTION

Manufactured by:
Samson Pharmaceuticals Inc.
Commerce, CA 90040

PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label

KILLS 99.99%
of GERMS

MADE IN
U.S.A.

Purita™

LA
Bodies™

Anti-Bacterial
HAND SANITIZER
with Moisturizer & Vitamin E

H1N1 Antiviral

NET WT 2 FL OZ (59 ml)

INGREDIENTS AND APPEARANCE

LA BODIES PURITA ANTI-BACTERIAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20146-4009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	620 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
propylene glycol (UNII: 6DC9Q167V3)
aloe vera leaf (UNII: ZY81Z83H0X)
glycerin (UNII: PDC6A3C0OX)
.alpha.-tocopherol acetate (UNII: 9E8X80D2L0)
carbomer homopolymer type c (allyl pentaerythritol crosslinked) (UNII: 4Q93RCW27E)
trolamine (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20146-4009-1	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2015
2	NDC: 20146-4009-2	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2015
3	NDC: 20146-4009-3	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2015

Labeler - SAMSON PHARMACEUTICAL (088169581)

Establishment
Name	Address	ID/FEI	Business Operations
SAMSON PHARMACEUTICAL		088169581	MANUFACTURE(20146-4009)