NELLIES HAND SANITIZER EUCALYPTUS- benzalkonium chloride liquid

Nellies Hand Sanitizer eucalyptus by

Drug Labeling and Warnings

Nellies Hand Sanitizer eucalyptus by is a Otc medication manufactured, distributed, or labeled by LAB-CLEAN, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Warnings

For External Use Only!

When using this product, avoid contact with eyes.

In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if 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

Uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use

Directions

Spray a small amount of product into palm of hand.

Rub thoroughly over all surfaces of both hands.

Rub hands together briskly until dry.

Inactive Ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid, Fragrance.

Package

INGREDIENTS AND APPEARANCE

NELLIES HAND SANITIZER EUCALYPTUS 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73126-007
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73126-007-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
2	NDC: 73126-007-02	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
3	NDC: 73126-007-03	710 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
4	NDC: 73126-007-04	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
5	NDC: 73126-007-05	3000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
6	NDC: 73126-007-06	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/22/2020

Labeler - LAB-CLEAN, INC (199822219)

Establishment
Name	Address	ID/FEI	Business Operations
LAB-CLEAN, INC		199822219	manufacture(73126-007)