PERSONAL CARE FOAMING HAND SANITIZER ROSEMARY LAVENDER- benzalkonium chloride liquid

Personal CARE Foaming Hand Sanitizer by

Drug Labeling and Warnings

Personal CARE Foaming Hand Sanitizer 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

to reduce bacteria on the skin.

Warnings

For external use only, hands only

When using this product

■ avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water ■ avoid contact with broken skin.

Stop use and ask a doctor if

■irritation or redness develops ■condition 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

■wet hands thoroughly with product and alllow to dry without wiping ■for children under 6, use only under adult supervision

Inactive ingredients

cetrimonium chloride, disodium cocoaphodiacetate, lavandula angustifolia (lavender) flower oil, methylchloroisothiazolinone, methylisothiazolinone, PEG-12 dimethicone, ploysorbate 20, tocopheryl acetate, water

Package Label

INGREDIENTS AND APPEARANCE

PERSONAL CARE FOAMING HAND SANITIZER  ROSEMARY LAVENDER
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-140
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 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
LAVENDER OIL (UNII: ZBP1YXW0H8)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-140-08	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/29/2020

Labeler - Delta Brands Inc (102672008)