OTC Medication Information: CVS Saline

CVS SALINE- sodium chloride spray
CVS PHARMACY

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.

Drug Facts Active Ingredients

Sodium Chloride 0.65%

Purpose

Moisturizer

Uses

provides instant, soothing relief to dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.

Warnings

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222

Directions

For children and adults, squeeze bottle twice in each nostril as often as needed or as directed by physician. For infants, use drop application. Hold bottle upright for spray, horizontally for stream, and upside down for drop. The use of this dispenser by more than one person may spread infection.

Other Information

store at room temperature

Inactive Ingredients

Aloe barbadensis leaf juice (aloe vera gel), benzalkonium chloride, benzyl alcohol, purified water, sodium phosphate dibasic, sodium phosphate monobasic

Questions or comments?

1-866-467-2748

*This product is not manufactured or distributed by Valeant Pharmaceuticals North America LLC, owners of the registered trademark Ocean®.

Distributed by:

Saline Nasal Spray

Compare to the ingredient in Ocean®*

NDC: 69842-438-30

Saline Nasal Spray

+ Soothing Aloe

Sodium Chloride 0.65%

Instantly relieves dry nasal passages caused by sinus, cold and allergy medications and dry air
Gentle enough for infants
Relief for stuffy noses

3 FL O.Z. (89 mL)

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL AROUND CAP IS BROKEN OR MISSING.

Distributed by:

CVS Saline Nasal Spray
(click image for full-size original)
CVS SALINE
nasal spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-438
Route of Administration NASAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM CHLORIDE (CHLORIDE ION) SODIUM CHLORIDE 6.5 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALOE VERA LEAF
BENZALKONIUM CHLORIDE
BENZYL ALCOHOL
WATER
SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM
SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69842-438-30 1 BOTTLE in 1 CARTON contains a BOTTLE
1 89 mL in 1 BOTTLE This package is contained within the CARTON (69842-438-30)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part349 02/15/2021
Labeler — CVS PHARMACY (062312574)

Revised: 06/2022 CVS PHARMACY

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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