ANTIMICROBIAL HAND SANITIZER- alcohol liquid

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]

Drug Facts

Active Ingredient

Ethyl Alcohol 66.5%

Purpose

Antiseptic

INDICATIONS & USAGE

Uses To reduce bacteria on the skin Recommended for repeated use

WARNINGS

Warnings

For external use only. Flammable, keep away from fire or flame.

DO NOT USE

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

ASK DOCTOR

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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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

INACTIVE INGREDIENT

Inactive Ingredients aloe vera, fragrance, purified water, triethanolamine

SPL UNCLASSIFIED SECTION

Antimicrobial Hand Sanitizer

Sprayer Fresh .** fl. oz.

Pkgd by HPC Global,

Hanover PA, 17331

Made in USA

Lot # ****

NDC:

51811-100-50

NDC:

51811-100-52

NDC:

51811-100-57

INGREDIENTS AND APPEARANCE

ANTIMICROBIAL HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51811-100(NDC:61010-3111)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	665 mL  in 1 L

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51811-100-50	0.008 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/01/2020
2	NDC: 51811-100-52	0.01 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2012
3	NDC: 51811-100-57	0.029 L in 1 BOTTLE, SPRAY; 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	05/21/2012

Labeler - HPC Ventures, LLC (097538103)