L’OCCITANE EN PROVENCE - LAVENDER SCENT HAND SANITIZER

L OCCITANE EN PROVENCE LAVENDER SCENT HAND SANITIZER by

Drug Labeling and Warnings

L OCCITANE EN PROVENCE LAVENDER SCENT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by LABORATOIRES M&L. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

L OCCITANE EN PROVENCE LAVENDER SCENT HAND SANITIZER- alcohol gel 
LABORATOIRES M&L

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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L’OCCITANE EN PROVENCE - LAVENDER SCENT HAND SANITIZER

Drug Facts

Active Ingredient

Ethyl alcohol 77% v/v

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame. For adult use only.

Do not use

on open skin wounds.

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if 

irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Water (Aqua), Glycerin, Ammonium Acryloyldimethyltaurate/VP Copolymer, Aloe Barbadensis Leaf Juice, Lavandula Angustifolia (Lavender) Oil, DMDM Hydantoin, Diazolidinyl Urea

Questions?

Call toll free 1 888 623 2880

Package Labeling:59ml

Package Labeling:236ml

L OCCITANE EN PROVENCE LAVENDER SCENT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10345-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.77 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
LAVENDER OIL (UNII: ZBP1YXW0H8)
DMDM HYDANTOIN (UNII: BYR0546TOW)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10345-103-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/23/2020	11/30/2022
2	NDC: 10345-103-02	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/23/2020	11/30/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/23/2020	11/30/2022

Labeler - LABORATOIRES M&L (262533623)

Revised: 11/2022

Document Id: ee95462f-d777-b513-e053-2a95a90af6a9

34390-5

Set id: b6ac04fb-0e10-745f-e053-2a95a90a362d

Version: 2

Effective Time: 20221128