DG BABY FOAMING HAND SANITIZER- benzalkonium chloride liquid 
Dolgencorp 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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Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

to decrease bacteria on the skin

Warnings

For external use only, hands only

When using this product

■ avoid contact with the 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 allow to dry without wiping ■ for children under 6, use only under adult supervision ■ not recommended for infants

Inactive ingredients

cetrimonium chloride, citrus reticulata X C. sinensis peel extract, disodium cocoamphodiacetate, PEG-12 dimethicone, tocopheryl acetate, water

Package Label

Package Label

DG BABY  FOAMING HAND SANITIZER
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-989
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
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
WATER (UNII: 059QF0KO0R)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55910-989-80236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/10/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/10/2019
Labeler - Dolgencorp Inc. (068331990)

Revised: 4/2019
Document Id: 86ad176c-013d-144f-e053-2a91aa0a986d
Set id: 86ad36a5-08b7-7792-e053-2a91aa0a2f6b
Version: 1
Effective Time: 20190416
 
Dolgencorp Inc.