Hand Sanitizer Wipes (BZK) - Soft Wet Wipes

Soft Wet Wipes by

Drug Labeling and Warnings

Soft Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Rite-Kem Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SOFT WET WIPES- soft wet wipes liquid 
Rite-Kem Incorporated

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Hand Sanitizer Wipes (BZK) - Soft Wet Wipes

Benzalkonium chloride 0.13%

Antiseptic

Hand Sanitizing Wipe to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

For external use only.

• In children less than 2 months of age
• on open skin wounds
• If you are allergic to any of the ingredients

Discontinue use if irritiation or redness develops. If conditions persist for more than 2 hours consult a physician.

Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a poison control center immediately.

Directions for Use:

• Thoroughly wipe hands with wipe.
• Discard in trash receptacle.
• Do not flush.
• Be sure to reseal label completely to retain moisture.

Other information

store between 15-30 c (59-86F)

Avoid freezing and excessing heat above 40 c (104F)

Inactive ingredients: Water, Propylene Glycol, Disodium EDTA, Chloromethylisothlazolinone, Methylisothiazolinone, Potassium Sorbate, Quaternium-15, Aloe Barbadansis Leaf Juice, Disodium Cocoamphodiacetate, Tocopheryl Acetate, Polysorbate-20, Citric Acid, Fragrance.

Soft Wet Wipes

(15 Count)

See Back Panel for Use Information

RITE-KEM

Sold by Rite-Kem Inc. T

703 Westmoreland Tupelo MS 38801

www.RITE-KEM.com

NDC: 73943-950-01

SOFT WET WIPES 
soft wet wipes liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73943-950
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)
CITRAL PROPYLENE GLYCOL ACETAL (UNII: 9W7YHX7EX6)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
ALOE (UNII: V5VD430YW9)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
QUATERNIUM-15 (UNII: E40U03LEM0)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73943-950-01	15 in 1 PACKAGE	05/17/2021	02/11/2025
1		2.1 g in 1 APPLICATOR; 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	05/17/2021	02/11/2025

Labeler - Rite-Kem Incorporated (786892927)

Establishment
Name	Address	ID/FEI	Business Operations
Rite-Kem Incorporated		786892927	manufacture(73943-950)

Revised: 2/2025

Document Id: 30e0d333-9cbe-5143-e063-6294a90a6ab1

34390-5

Set id: c24e99b8-0051-74d7-e053-2a95a90a0ce4

Version: 17

Effective Time: 20250212