F&F Wipe-Off Gym Wipes

Hand Sanitizing Wipes by

Drug Labeling and Warnings

Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Hangzhou Linkeweier Daily Chemicals Co. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZING WIPES- benzalkonium chloride swab 
Hangzhou Linkeweier Daily Chemicals Co. Ltd.

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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F&F Wipe-Off Gym Wipes

ACTIVE INGREDIENT

Benzalkonium chloride 0.08%

PURPOSE

Antiseptic

USES

• For handwashing to decrease bacteria on the skin.
• After changing diapers.
• After assisting ill persons.
• Before contact with a person under medical care or treatment.
• Recommended for repeat use.

WARNING

For external use only.

Do not use in the eyes.

WHEN USING THIS PRODUCT

When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.

STOP USE AND ASK A DOCTOR IF

Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach from children. If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

• Wet hands thoroughly with product and allow to dry.
• Children under six years of age should be supervised when using this product.

OTHER INFORMATION

Store in a cool, dry place.

INACTIVE INGREDIENT

Decyl Glucoside，Polyaminopropyl Biguanide，Phenoxyethanol， Didecyl Dimethyl Ammonium Chloride，Aloe Barbadensis Leaf Juice Glyceri，Vitamin E, Water

PACKAGE LABEL

800 IN A BAG NDC: 71766-004-01

HAND SANITIZING WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71766-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.08   in 100

Inactive Ingredients
Ingredient Name	Strength
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71766-004-01	800 in 1 BAG; Type 0: Not a Combination Product	02/12/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/12/2021

Labeler - Hangzhou Linkeweier Daily Chemicals Co. Ltd. (544544821)

Registrant - Hangzhou Linkeweier Daily Chemicals Co. Ltd. (544544821)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Linkeweier Daily Chemicals Co. Ltd.		544544821	manufacture(71766-004) , label(71766-004)

Revised: 2/2021

Document Id: bb1f9a96-4eba-6dd6-e053-2a95a90a6248

34390-5

Set id: bb1f9a96-4eb9-6dd6-e053-2a95a90a6248

Version: 1

Effective Time: 20210212

 

Hang