PERSONAL CARE FOAMING HAND SANITIZER ROSEMARY LAVENDER- benzalkonium chloride liquid 
Delta Brands 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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Personal CARE Foaming Hand Sanitizer

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

Package Label

PERSONAL CARE FOAMING HAND SANITIZER  ROSEMARY LAVENDER
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-140
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:20276-140-08236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/29/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/29/2020
Labeler - Delta Brands Inc (102672008)

Revised: 6/2023
 
Delta Brands Inc