99X by Southern Products and Services, Inc

99X by

Drug Labeling and Warnings

99X by is a Otc medication manufactured, distributed, or labeled by Southern Products and Services, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

99X- benzalkonium chloride liquid 
Southern Products and Services, 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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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


Pump a small amount of foam into palm of hand
Rub thoroughly over all surfaces of both hands
Rub hands together briskly until dry

Inactive Ingredients

Water, cocamidopropyl PG-dimonium chloride phosphate, dihydroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid

Principal Display Panel

99X 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 82738-250
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)  
WATER (UNII: 059QF0KO0R)  
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
Product Characteristics
Colorwhite (Clear Colorless) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 82738-250-413785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/19/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/19/202207/19/2022
Labeler - Southern Products and Services, Inc (011085205)

Revised: 8/2022
Document Id: e5fd29f0-c755-553a-e053-2a95a90a1b0a
Set id: e42e8855-2dbd-58b1-e053-2995a90a27a1
Version: 2
Effective Time: 20220811