ANTIMICROBIAL HAND SANITIZER- alcohol gel

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 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

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

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

SPL UNCLASSIFIED SECTION

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

NDC:

51811-300-20

NDC:

51811-300-21

NDC:

51811-300-25

NDC:

51811-300-31

NDC:

51811-300-40 and 51811-300-41

NDC:

51811-300-44 and 51811-300-45

NDC:

51811-300-50

NDC:

51811-300-51 and 51811-300-52

INGREDIENTS AND APPEARANCE

ANTIMICROBIAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51811-300(NDC:61010-4111)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51811-300-20	29 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/01/2020
2	NDC: 51811-300-21	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2010
3	NDC: 51811-300-25	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2010
4	NDC: 51811-300-31	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2010
5	NDC: 51811-300-40	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2010
6	NDC: 51811-300-41	118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/20/2010
7	NDC: 51811-300-44	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/20/2010
8	NDC: 51811-300-45	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/20/2010
9	NDC: 51811-300-50	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/20/2010
10	NDC: 51811-300-51	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2020
11	NDC: 51811-300-52	473 mL in 1 BOTTLE, PUMP; 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	12/20/2010

Labeler - HPC Ventures, LLC (097538103)