Label: SALINE- nasal spray
- NDC Code(s): 68163-704-15
- Packager: Raritan Pharmaceuiticals Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 29, 2025
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- Active Ingredients
- Purpose
- Uses
- Warnings
- Keep out of reach of children.
- Directions
- Other Information
- Inactive Ingredients
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Saline Nasal Spray
Compare to the active ingredient in Ocean®*
DRx Choice
NDC: 68163-704-15
Saline Nasal Spray
Sodium Chloride 0.65%
Instantly relieves dry nasal passages caused by sinus, cold and allergy medications and dry air
Safe for frequent daily use
Gentle enough for infants
Natural, non-medicated relief for stuffy noses
100% SATISFACTION GUARANTEED OR YOUR MONEY BACK
1.5 FL O.Z. (44 mL)
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL AROUND CAP IS BROKEN OR MISSING.
DISTRIBUTED BY:
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INGREDIENTS AND APPEARANCE
SALINE
nasal sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68163-704 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 BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BENZYL ALCOHOL (UNII: LKG8494WBH) WATER (UNII: 059QF0KO0R) SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74) SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68163-704-15 1 in 1 CARTON 09/30/2020 1 44 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 09/30/2020 Labeler - Raritan Pharmaceuiticals Inc (127602287)

