FAMILY CARE SALINE- sodium chloride spray

Family Care Saline by

Drug Labeling and Warnings

Family Care Saline by is a Otc medication manufactured, distributed, or labeled by United Exchange Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient Purpose

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

PURPOSE

Use

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

WARNINGS

Warnings

For external use only

PREGNANCY OR BREAST FEEDING

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

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

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

STORAGE AND HANDLING

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 INGREDIENT

Inactive ingredients

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

DOSAGE & ADMINISTRATION

Distributed by: United Exchange Corp.

Cypress, CA 90630 USA

Made in China

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FAMILY CARE SALINE 
sodium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-493
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	6.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
BENZYL ALCOHOL (UNII: LKG8494WBH)
WATER (UNII: 059QF0KO0R)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-493-44	44 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/28/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	09/28/2023

Labeler - United Exchange Corp. (840130579)