ANTIMICROBIAL HAND SANITIZER- alcohol gel 
HPC Ventures, LLC

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Antimicrobial Hand Sanitizer - Unscented

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

Warnings

For external use only

Flammable, keep away from fire or flame

Do not use in the eyes, if this happens reinse thoroughly with water.

Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours

Keep out of reach of children

If ingested get medical help or contact a Poison Control Center right away

Directions

Inactive Ingredients aloe vera, carbomer, purified water, triethanolamine

Antimicrobial Hand Sanitizer Gel - Unscented ** fl. oz. Lot# ****

Pkgd by HPC Global, Hanover PA, 17331 Made in USA

NDC 51811-400-20

LABEL NDC 51811-400-20

NDC 51811-400-21

NDC 51811-400-21

NDC 51811-400-25

NDC 51811-400-25

NDC 51811-400-31

NDC 51811-400-31

NDC 51811-400-40 and 51811-400-41

NDC 51811-400-40 and 51811-400-41

NDC 51811-400-44 and 51811-400-45

NDC 51811-400-44 and 51811-400-45

NDC 51811-400-50

NDC 51811-400-50

NDC 51811-400-51 and 41811-400-52

NDC 51811-400-51 and 51811-400-52

ANTIMICROBIAL HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51811-400(NDC:61010-7111)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 L
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51811-400-200.029 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2020
2NDC:51811-400-210.029 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
3NDC:51811-400-250.029 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
4NDC:51811-400-310.059 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
5NDC:51811-400-400.118 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
6NDC:51811-400-410.118 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/13/2010
7NDC:51811-400-440.236 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
8NDC:51811-400-450.236 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/13/2010
9NDC:51811-400-500.473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/13/2010
10NDC:51811-400-510.473 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2020
11NDC:51811-400-520.473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00309/13/2010
Labeler - HPC Ventures, LLC (097538103)

Revised: 12/2024
Document Id: 0d84ba89-caec-f78e-e063-6294a90ae277
Set id: da7ef222-b38b-fee2-e053-2995a90affd8
Version: 3
Effective Time: 20241227
 
HPC Ventures, LLC