LA BODIES PURITA ANTI-BACTERIAL HAND SANITIZER- alcohol gel 
SAMSON PHARMACEUTICAL

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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LA Bodies™ Purita™ Anti-Bacterial Hand Sanitizer

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

  • 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.

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)

PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label
LA BODIES PURITA ANTI-BACTERIAL HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20146-4009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol620 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:20146-4009-159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2015
2NDC:20146-4009-2236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2015
3NDC:20146-4009-3473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2015
Labeler - SAMSON PHARMACEUTICAL (088169581)
Establishment
NameAddressID/FEIBusiness Operations
SAMSON PHARMACEUTICAL088169581MANUFACTURE(20146-4009)

Revised: 1/2022
Document Id: bef25793-66c3-4464-9631-03858e5fe3d9
Set id: 241662eb-8b12-4413-9ece-6c9a0d7bbe82
Version: 4
Effective Time: 20220131
 
SAMSON PHARMACEUTICAL