Active Ingredient

Alcohol 70% by volume

Purpose

Antiseptic

Uses

• For hand sanitizing to decrease bacteria on the skin.
• Apply topically to the skin to help prevent cross contamination.
• Recommended for repeated use.
• Dries In seconds.

Warnings

Flammable, keep away from fire or flame. For external use only.
Do not use In or contact the eyes.
Discontinue use If redness or Irritation develops.
If condition persists for more than 72 hours, consult a physician.

Keep our of reach of children

Keep out of reach of chlldren unless under adult supervision.

Directions

•Remove lld.
• Pull wipe from center of roll and thread through opening in lid. Do not
push finger through opening.
• Replace lld, pull wipe up, and then out at 45 • angle. The next wipe
dispenses automatically.
• Close lld to retain moisture.

Inactive Ingredients

Water, Propylene Glycol, Glycerin, Carboner, Aminomethyl Propanol, Aloe Barbadenis Leaf Juice, Tocopheryl Acetate.

Questions or Comments

Lot No. and Expiration Date can be found on canister.

@PROGRESSIVE PRODUCTS, LLC
4 International Drive, Rye Brook, NY 1 0573
CGll 914-417-6022
Re-order/Item No. 33884
www.wlpesplus.com

Principal Display Panel

NDC 67151-606-01

RE-ORDER/ITEM NO 37604

Label

NDC 67151-606-02

RE-ORDER/ITEM NO 33884

Label 1

NDC 67151-606-03

RE-ORDER/ITEM NO 37524

Label 2

WIPES PLUS
alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67151-606
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:67151-606-01	80 in 1 PACKAGE	09/01/2020
1		1 mL in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC:67151-606-02	240 in 1 PACKAGE	09/01/2020
2		1 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC:67151-606-03	1500 in 1 PACKAGE	09/01/2020
3		1 mL in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	09/01/2020

Labeler - Progressive Products, LLC (127111792)

Registrant - Progressive Products, LLC (127111792)

DRUG FACTS