LAVENDER HAND SANITIZER- benzalkonium chloride spray

United States - English - NLM (National Library of Medicine)

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Active ingredient:
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
Available from:
Mangiacotti, Inc
Administration route:
TOPICAL
Prescription type:
OTC DRUG
Therapeutic indications:
- For hand sanitizing to decrease bacteria on the skin - Recommended for repeated use
Authorization status:
OTC monograph not final
Authorization number:
42926-007-01

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LAVENDER HAND SANITIZER- benzalkonium chloride spray

Mangiacotti, 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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Lavender Hand Sanitizer Spray

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

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.

Directions

Spray a small amount into palm of hands

Rub thoroughly over all surfaces of both hands

Rub hands together briskly until dry

Inactive Ingredients

Water, cetrimonium chloride, lautrimonium chloride, dihydroxyethyl cocamine oxide,

glycereth-17 cocoate, citric acid, fragrance with essential oils

Package Labeling:

LAVENDER HAND SANITIZER

benzalkonium chloride spray

Product Information

Product Type

HUMAN OTC DRUG

Item Code (Source)

NDC:42926-007

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Strength

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -

UNII:7N6JUD5X6Y)

BENZ ALKONIUM

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:42926-007-

1 in 1 TUBE

12/21/2020

1

9 mL in 1 BOTTLE; Type 0: Not a Combination

Product

Marketing Information

Marketing

Category

Application Number or Monograph

Citation

Marketing Start

Date

Marketing End

Date

OTC monograph not

part333E

12/21/2020

Mangiacotti, Inc

final

part333E

12/21/2020

Labeler -

Mangiacotti, Inc (078850804)

Revised: 7/2021

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