ANTIMICROBIAL HAND SANITIZER- alcohol gel 
HPC Ventures, LLC

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Antimicrobial Hand Sanitizer - Fresh Scent

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

For handwashing to decrease bacteria on skin

Fecommended for repeated use

Warnings

For external use only

Flammable, keep away from fire or flame

Do not use in the eyes, if this happens rinse 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, D&C green #5, D&C yellow #10, fragrance, purified water, thriethanolamine

Antimicrobial Hand Sanitizer Gel - Fresh ** fl. oz. Lot# ****
Pkgd by HPC Global, Hanover PA, 17331 Made in USA

NDC 51811-300-20

51811-300-20

NDC 51811-300-21

51811-300-21

NDC 51811-300-25

51811-300-25

NDC 51811-300-31

51811-300-31

NDC 51811-300-40 and 51811-300-41

51811-300-40 and 51811-300-41

NDC 51811-300-44 and 51811-300-45

51811-300-44 and 51811-300-45

NDC 51811-300-50

NDC 51811-300-50

NDC 51811-300-51 and 51811-300-52

NDC 51811-300-51 and 51811-300-52

ANTIMICROBIAL HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51811-300(NDC:61010-4111)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
WATER (UNII: 059QF0KO0R)  
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51811-300-2029 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2020
2NDC:51811-300-2129 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/20/2010
3NDC:51811-300-2529 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/20/2010
4NDC:51811-300-3159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/20/2010
5NDC:51811-300-40118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/20/2010
6NDC:51811-300-41118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/20/2010
7NDC:51811-300-44236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/20/2010
8NDC:51811-300-45236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/20/2010
9NDC:51811-300-50473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/20/2010
10NDC:51811-300-51473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2020
11NDC:51811-300-52473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00312/20/2010
Labeler - HPC Ventures, LLC (097538103)

Revised: 12/2024
Document Id: 0d84b7f8-728a-ae75-e063-6394a90a72ab
Set id: de079eb4-dfd6-1c4a-e053-2a95a90af116
Version: 3
Effective Time: 20241227
 
HPC Ventures, LLC