NELLIES BABY LAVENDER- benzalkonium chloride liquid
LAB-CLEAN, 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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Nellie’s Baby Lavender

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

image description

NELLIES BABY LAVENDER
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73126-005
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:73126-005-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
2	NDC:73126-005-02	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
3	NDC:73126-005-03	710 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
4	NDC:73126-005-04	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
5	NDC:73126-005-05	3000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
6	NDC:73126-005-06	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020
7	NDC:73126-005-07	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/22/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	05/22/2020	04/20/2024

Labeler - LAB-CLEAN, INC (199822219)

Name	Address	ID/FEI	Business Operations
Establishment
LAB-CLEAN, INC		199822219	manufacture(73126-005)

Revised: 4/2022

Document Id: dd937274-7fbf-2339-e053-2a95a90a74eb

Set id: 8990704e-4885-44c0-aefa-e8018aeb89c3

Version: 4

Effective Time: 20220426

LAB-CLEAN, INC