HILL COUNTRY FARE HAND SANITIZER

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by H.E.B. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER HILL COUNTRY FARE- alcohol aerosol, spray 
H.E.B

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HILL COUNTRY FARE HAND SANITIZER

Active Ingredient(s)

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

• hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

For external use only.

Flammable.

Keep away from heat or flame. Do not use while smoking.

Do not use

• on children less than 2 months of age
• on open skin wounds

When using this product

• keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water to remove.
• do not puncture or incinerate. Contents under pressure. Do not store at temperatufes above 120ºF.

Stop use and ask a doctor if

rash or irritation occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• spray enough product in palm to thoroughly cover your hands
• rub hands together briskly until dry
• children under 6 years of age should be supervised when using this product.

Other information

• may discolor or damage some fabrics/materials or surfaces.
• avoid freezing and excessive heat above 40ºC (104ºF).

Inactive ingredients

water, glycerin, aloe barbadensis leaf juice, tocopheryl acetate

HAND SANITIZER  HILL COUNTRY FARE
alcohol aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-287
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mg  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-287-37	156 g in 1 CAN; Type 0: Not a Combination Product	04/14/2020
2	NDC: 37808-287-74	76.5 g in 1 CAN; Type 0: Not a Combination Product	04/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	04/14/2020	12/23/2022

Labeler - H.E.B (007924756)

Revised: 10/2024

Document Id: 24898f7f-5bae-5e70-e063-6394a90a91cc

34390-5

Set id: aa532217-64d2-1ee2-e053-2a95a90af779

Version: 3

Effective Time: 20241015