FAMILY CARE SALINE- sodium chloride spray 
United Exchange Corp.

----------

Active ingredient Purpose

Sodium Chloride 0.65%......................Moisturizer

Use

temporary relief of dry, irritated nasal passages due to colds, flu, allergies, pollution, and the use of decongestants/steroidal sprays

Warnings

For external use only

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

  • holding bottle upright for spray, horizontally for stream, and upside down for drop applications
  • adults and children under 6 years of age: squeeze twice in each nostril as needed
  • children under 6 years of age: consult a doctor
  • using this dispenser by more than one person may spread infection

Other information

  • store at room temperature 20-25°C (68-77°F)
  • do not use if printed seal around the cap is broken or missing

Inactive ingredients

benzalkonium chloride, benzyl alcohol, purified water, sodium phosphate dibasic anhydrous, sodium phosphate monobasic monohydrate

Distributed by: United Exchange Corp.

Cypress, CA 90630 USA

Made in China

493

FAMILY CARE SALINE 
sodium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-493
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE6.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)  
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
WATER (UNII: 059QF0KO0R)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65923-493-4444 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/28/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01209/28/2023
Labeler - United Exchange Corp. (840130579)

Revised: 9/2023
Document Id: 06737393-d4af-3e7b-e063-6394a90ac19f
Set id: 06737393-d4ae-3e7b-e063-6394a90ac19f
Version: 1
Effective Time: 20230928
 
United Exchange Corp.