EVERYWHERE FLUSHABLE WIPES cloth

Everywhere Flushable Wipes by

Drug Labeling and Warnings

Everywhere Flushable Wipes by is a Otc medication manufactured, distributed, or labeled by Shenzhen Shierjie Biological Engineering Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

BENZALKONIUM CHLORIDE 0.15%

Purpose

Antimicrobial

Use

1 Gently cleanses external intimate areas (perianal & vulvar regions),
reduces bacteria on skin surfaces.
2.For personal hygiene after toileting or during menstrual care.

Warnings

FOR EXTERNAL USE ONLY. Disposable wipes, one time use only.

Do not use

1. If you are allergic to any ingredient in this product.
2. If packaging seal is compromised.
3. As a substitute for medical treatment.

When Using

Avoid contact with eyes, lips, and mouth. If contact occurs,
rinse thoroughly with water.

Stop Use

STOP USE and ask a doctor if:
Burning, swelling, or unusual discharge occurs

Keep Oot Of Reach Of Children

To avoid the risk of chocking and suffocation, keep wipes and
plastic bag away from babieschildren and pets.

Directions

1.Wash hands before use
2.Unfold wipe without tearing
3.Gently wipe external intimate areas from front to back
4.rinse-free.

Other information

Not have

Inactive ingredients

Water, Glycerin, Propylene glycol, Polysorbate 20，
Phenoxyethanol, Octanediol, Aloe barbadensis Extract, Lactic acid，
Chrysanthellum Indicum Extract, Fragrance, Citrus Aurantium Dulcis
(Orange) Fruit extract, Ethylhexylglycerin, 1 ,2-Hexanediol,
Hydroxyacetophenone

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EVERYWHERE FLUSHABLE WIPES 
everywhere flushable wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43116-042
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.15 U  in 100 U

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
OCTANEDIOL (UNII: 806K32R50Z)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
LACTIC ACID, L- (UNII: F9S9FFU82N)
CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0)
CITRUS AURANTIUM DULCIS (ORANGE) FRUIT POWDER (UNII: 5EVU04N5QU)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
CLOVE (UNII: K48IKT5321)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43116-042-01	30 U in 1 BOX; Type 0: Not a Combination Product	06/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	06/09/2025

Labeler - Shenzhen Shierjie Biological Engineering Co., LTD (547610261)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Shierjie Biological Engineering Co., LTD		547610261	manufacture(43116-042)