BONBLISSITY HAND SANITIZING WIPES- benzalkonium chloride cloth
BONBLISS BEAUTY, INC.

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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73582-0002_BONBLISSITY HAND SANITIZING WIPES

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria

Warnings

For external use only

When using this product do not use in or near the eyes. If contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation develops and 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

For use apply thoroughly to hands as desired. Allow to dry without wiping. Discard wipe in trash receptacle after use. Do not flush.

For dispensing peel back front label at tab. Remove towelettes as needed. Reseal pouch by pressing label firmly back into place.

Inactive ingredients

Water, Phenoxyenthanol, Glycerin, Sodium Benzoate, Polysorbate 20, Disodium EDTA, Citric Acid, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract, Fragrance

Product Label

BONBLISSITY HAND SANITIZING WIPES
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73582-0002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.01 g in 1 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:73582-0002-1	58 g in 1 POUCH; Type 0: Not a Combination Product	06/02/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	06/02/2020

Labeler - BONBLISS BEAUTY, INC. (055735749)

Registrant - BONBLISS BEAUTY, INC. (055735749)

Name	Address	ID/FEI	Business Operations
Establishment
FIRSTCHAM CO., LTD		694707327	manufacture(73582-0002)