PERSONAL CARE WET WIPES CITRUS- benzalkonium chloride cloth

Personal CARE Wet Wipes by

Drug Labeling and Warnings

Personal CARE Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Delta Brands, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Uses

for hand sanitizing to decrease bacteria on skin

Warnings

For external use only

Do not use

if you are allergic to any of the ingredients

When using this product

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

irritation or rash develops and continues 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

adults and children 2 years and over ■ apply to hands ■ allow to dry without wiping

children under 2 years ask a doctor before use

Inactive ingredients

water, ethyl alcohol, aloe barbadensis leaf juice, PEG-60 lanolin, fragrance, tetrasodium EDTA, phenoxyethanol, potassium sorbate, quaternium-52, citric acid

Package Label

INGREDIENTS AND APPEARANCE

PERSONAL CARE WET WIPES  CITRUS
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-436
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

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
PEG-60 LANOLIN (UNII: K2OI1D27ET)
QUATERNIUM-52 (UNII: 588EQF3H1P)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-436-15	15 in 1 BOX	01/07/2021
1	NDC: 20276-436-01	1 in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 20276-436-18	18 in 1 BOX	01/07/2021
2	NDC: 20276-436-01	1 in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 20276-436-30	30 in 1 BOX	01/07/2021
3	NDC: 20276-436-01	1 in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 20276-436-40	40 in 1 BOX	01/07/2021
4	NDC: 20276-436-01	1 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/07/2021

Labeler - Delta Brands, Inc (102672008)