Antimicrobial Hand Sanitizer - Unscented

Antimicrobial Hand Sanitizer by

Drug Labeling and Warnings

Antimicrobial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by HPC Ventures, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• For handwashing to decrease bacteria on skin
• Recommended for repeated use

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

• wet hands thoroughly with product allow to dry without wiping
• children under six should be supervised while using this product

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

NDC: 51811-400-21

NDC: 51811-400-25

NDC: 51811-400-31

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

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

NDC: 51811-400-50

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

ANTIMICROBIAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51811-400(NDC: 61010-7111)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	700 mg  in 1 L

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51811-400-20	0.029 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/01/2020
2	NDC: 51811-400-21	0.029 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/13/2010
3	NDC: 51811-400-25	0.029 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/13/2010
4	NDC: 51811-400-31	0.059 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/13/2010
5	NDC: 51811-400-40	0.118 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/13/2010
6	NDC: 51811-400-41	0.118 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/13/2010
7	NDC: 51811-400-44	0.236 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/13/2010
8	NDC: 51811-400-45	0.236 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/13/2010
9	NDC: 51811-400-50	0.473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/13/2010
10	NDC: 51811-400-51	0.473 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/01/2020
11	NDC: 51811-400-52	0.473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/13/2010	08/13/2025

Labeler - HPC Ventures, LLC (097538103)

Revised: 6/2025

Document Id: 3c4350ea-c3f6-12ad-e063-6394a90a6402

34390-5

Set id: da7ef222-b38b-fee2-e053-2995a90affd8

Version: 4

Effective Time: 20250627