Zuum Klin Gel Antibacterial

Zuum Klin Antibacterial by

Drug Labeling and Warnings

Zuum Klin Antibacterial by is a Otc medication manufactured, distributed, or labeled by U.S. Cotton Mexico, S. de R.L. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ZUUM KLIN ANTIBACTERIAL- alcohol gel 
U.S. Cotton Mexico, S. de R.L. de C.V.

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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Zuum Klin Gel Antibacterial

Drug Facts

Active ingredient

Ethyl alcohol 63%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only

Flammable, keep away from fire or flame

Do not use

in the eyes

Stop use and ask a doctor

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

wet hands thoroughly with product and allow to dry without wiping

Other information

Keep this product away from heat, fire or sunlight.

Inactive ingredients

Isopropyl alcohol, deionized water, aloe vera (aloe barbadensis) extract, propylene glycol, carbomer, aminomethyl propanol, fragrance, EDTA, vitamin E, vitamin A, ceramides

Questions or Comments?

505-962-3014

Package Labeling:

ZUUM KLIN ANTIBACTERIAL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77388-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.63 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
EDETIC ACID (UNII: 9G34HU7RV0)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
VITAMIN A (UNII: 81G40H8B0T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77388-001-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2020

Labeler - U.S. Cotton Mexico, S. de R.L. de C.V. (816167605)

Establishment
Name	Address	ID/FEI	Business Operations
U.S. Cotton Mexico, S. de R.L. de C.V.		816167605	manufacture(77388-001)

Revised: 11/2020

Document Id: b4de1d26-6bcc-76ed-e053-2a95a90a4b03

34390-5

Set id: aa57fa0c-beb4-3022-e053-2995a90a76ee

Version: 3

Effective Time: 20201124