Alcohol Wet Wipes, 70 Alcohol

Alcohol Wet Wipes, 70 Alcohol by

Drug Labeling and Warnings

Alcohol Wet Wipes, 70 Alcohol by is a Otc medication manufactured, distributed, or labeled by Sweda Company LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALCOHOL WET WIPES, 70 ALCOHOL- alcohol cloth 
Sweda Company LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Alcohol Wet Wipes, 70 Alcohol

Drug Facts

Active Ingredient

Alcohol(70.00% V/V)

Purpose

Antiseptic

Uses

• For hand-washing to decrease bacteria on the skin

Warnings

Flammable. Keep away from heat and flame.

For External use only

Do not use

in eyes. In case of contact, rinse thoroughly with water.

Stop use & ask doctor

if rash/redness or irritation appears/develops and persists for more than 72 hours.

Keep out of reach of children

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

Directions

• Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation.
• Thoroughly wipe hands, allow to dry out rinsing. Discard after single use  

Other information

• Do not flush down toilet.
• Keep away from sunlight.Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit)
• May discolor certain fabrics

Inactive Ingredients

Aqua, Glycerin, Aloe Barbadensis Leaf Juice, D- Panthenol, Phenoxyethanol

Package Labeling:

ALCOHOL WET WIPES, 70 ALCOHOL 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90121-001
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DEXPANTHENOL (UNII: 1O6C93RI7Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90121-001-15	15 in 1 BAG	07/30/2020	01/01/2021
1		3.6 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/30/2020	01/01/2021

Labeler - Sweda Company LLC (081729899)

Revised: 2/2021

Document Id: bb61c361-fd3a-1748-e053-2995a90a7153

34390-5

Set id: ad53cd9a-64fb-9af3-e053-2995a90ae15d

Version: 2

Effective Time: 20210215