MEDI-WIPES- ethyl alcohol, chloroxylenol swab

MEDI-WIPES by

Drug Labeling and Warnings

MEDI-WIPES by is a Otc medication manufactured, distributed, or labeled by Afassco Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active Ingredients

Ethyl Alcohol 40.0%

Chloroxylenol (PCMX) 0.5%

Purpose

Antiseptic

Uses:

For hand washing to decrease bacteria on skin when soap and water are not available.

Warnings:

For external use only.

Flammable. Keep away from fire or flame

Directions:

• tear packet open, remove towelette
• wipe hands/wrist areas for 15 seconds and discard
  

When Using The Product:

• do not get into eyes. If contact occurs rinse eye thoroughly with water
  

Stop Use And Ask Doctor If:

• irritation or redness develop and persist for more than 72 hours
  

Inactive Ingredients:

aloe vera, fragrance, purified water

Keep Out Of Reach Of Children

Keep Out Of Reach Of Children:

If swallowed, get medical help or contact a Poison Control center right away. 1-800-222-1222

Product Label Medi-Wipes

MEDI-WIPES

Antimicrobial Towelette With PCMX and ALOE

Afassco::® The First Choice In First Aid

Manufactured for Afassco Inc, Minden, NV 89423 1.800.441.6774

Non-Drying
Meets OSHA Requirements
Decreases Bacteria On Skin
Use For Hand Washing When Soap And Water Are Not Available

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INGREDIENTS AND APPEARANCE

MEDI-WIPES 
ethyl alcohol, chloroxylenol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51532-5104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.6 g  in 1.5 g
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	7.5 g  in 1.5 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51532-5104-1	20 in 1 BOX	12/01/2013
1		1.5 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 51532-5104-2	500 in 1 BOX	12/01/2013
2		1.5 g in 1 PACKET; 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	part333E	12/01/2013

Labeler - Afassco Inc (609982723)

Registrant - Afassco Inc (609982723)