UNITED CLEANPLUS- sanitizing wipe cloth

United CleanPlus by

Drug Labeling and Warnings

United CleanPlus by is a Otc medication manufactured, distributed, or labeled by RMT Global Partners, LLC, Yangzhou Suxiang Medical Instrument Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Isopropyl Alcohol 750% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

To reduce bacteria on the skin.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

On open skin wounds

WHEN USING

Do not use in or near the eyes. In case of contact with eyes flush thoroughly with water.

Use wipes only on unbroken, intact skin

Do not ingest

STOP USE

If skin irritation or redness develops

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.

Directions

Wipe hands thoroughly, let skin dry and discard

Keep out of reach of children. Children under 6 years of age use only under adult supervision

Not recommended for infants

Do not store above 105°F

Inactive ingredients

pure water

Package Label - Principal Display Panel

1 PSC NDC: 80436-004-01

INGREDIENTS AND APPEARANCE

UNITED CLEANPLUS 
sanitizing wipe cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80436-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80436-004-06	1 in 1 PACKET	09/02/2020
1		1 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 80436-004-07	25 in 1 BOX	09/02/2020
2		25 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 80436-004-08	100 in 1 BOX	11/30/2020
3		100 mL in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 80436-004-09	100 in 1 POUCH	01/14/2022
4		100 mL in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 80436-004-10	100 in 1 CANISTER	01/14/2022
5		100 mL 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 Drug	M003	09/02/2020

Labeler - RMT Global Partners, LLC (060652584)

Establishment
Name	Address	ID/FEI	Business Operations
Yangzhou Suxiang Medical Instrument Co., Ltd		543387280	manufacture(80436-004)