HAND SANITIZING WIPES- ethyl alcohol cloth

Hand Sanitizing Wipes by

Drug Labeling and Warnings

Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by N A Artis Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 75% v/v.

Purpose

Antiseptic

Warnings

For external use only.

Flammable, keep away from heat or flame.

Do not use

• on open skin wounds.

When using this product, keep out of eyes, ears and mouth. In case of contact with eyes,rinse thoroughly with water immediately.

Stop using and consult a doctor if irritation or rash occurs, these may be sighs of a serious condition.

• Discard used wipes immediately to prevent cross contamination.
• Children should be under adult supervision when using this product.
• Not recommended for infants.

Keep out of reach of children.

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

Uses

• Decrease bacteria on the skin that could cause disease.
• For use when soap and water are not available.

Directions

• Open the pouch.
• Pull out wipe and close the pouch.
• Unfold and wipe hands, fingers and wrists thoroughly and allow to dry.
• For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe.
• Discard after single use.
• Make sure to close the pouch firmly after use to retain moisture.

Other Information

• Store between 59-86℉(15-30℃)
• Avoid freezing and excessive heat above 104℉ (40℃)
• May discolor some fabrics.
• Harmful to wood finishes and plastics.
• Lot number and expiry date can be found on packet.
• Dispose of wipe in proper container after use.
• Do not flush.

Inactive Ingredients

Water, Propylene Glycol, Glycerin, Aloe Vera, Vitamin E

Image

INGREDIENTS AND APPEARANCE

HAND SANITIZING WIPES 
ethyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79798-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ALOE (UNII: V5VD430YW9)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79798-001-01	5 in 1 PACKET	07/23/2020
1		3.6 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
2	NDC: 79798-001-02	10 in 1 PACKET	07/23/2020
2		3.6 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
3	NDC: 79798-001-03	20 in 1 PACKET	07/23/2020
3		3.6 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
4	NDC: 79798-001-04	50 in 1 PACKET	07/23/2020
4		3.6 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
5	NDC: 79798-001-05	80 in 1 PACKET	07/23/2020
5		3.6 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
6	NDC: 79798-001-06	80 in 1 CANISTER	07/23/2020
6		3.6 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
7	NDC: 79798-001-07	160 in 1 CANISTER	07/23/2020
7		3.6 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/23/2020

Labeler - N A Artis Inc (081009519)