Indications and uses
Naturally provides instant, soothing relief dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.
Saline Nasal Spray
- Manufacturer
- DISCOUNT DRUG MART, INC.
- Effective date
- 2022-01-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:47:36
Label at a glance#
ProductSaline
Active ingredientSODIUM CHLORIDE
Label structure10 sections
Dosage and administration
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.
Contacts and useful links#
Label contents#
Full prescribing information#
Active Ingredients
Sodium Chloride 0.65%
Purpose
Moisturizer
Uses
Naturally provides instant, soothing relief 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. Use of this container by more than one person may spread infection.
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
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, sodium phosphate monobasic.
Saline Nasal Spray
Compare to the active ingredient in Ocean®*
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
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL AROUND CAP IS BROKEN OR MISSING.
Distributed by:
Package label for 44 mL
Package Label for 88 mL
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 53943-704-15 | 2024-01-30 | C162847 | 48780-1 | 1030e365-4fc2-111a-e063-dadaa90a10e2 | Saline Nasal Spray |
| 53943-704-30 | 2024-01-30 | C162847 | 48780-1 | 1030e365-4fc2-111a-e063-dadaa90a10e2 | Saline Nasal Spray |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53943-704-15 | Saline | 1 in 1 CARTON | SPRAY | 1 | 2 | |
| 53943-704-15 | Saline | 44 mL in 1 BOTTLE | SPRAY | 44 | 2 | |
| 53943-704-30 | Saline | 1 in 1 CARTON | SPRAY | 1 | 2 | |
| 53943-704-30 | Saline | 88 mL in 1 BOTTLE | SPRAY | 88 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Saline
- Nasal
- SODIUM CHLORIDE
- CHLORIDE ION
- BENZALKONIUM CHLORIDE
- BENZYL ALCOHOL
- WATER
- SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM
- SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53943-704 | 53943-704-15, 53943-704-30 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM | GR686LBA74 | IACT |
| SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM | 3980JIH2SW | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 26f66d1c-bc7c-4cd5-ae15-663614cb6d82 | aa5bfec5-5ff6-4de5-b5dc-c1d6dcc6159c | 2022-01-25 | Warnings | 26f66d1c-bc7c-4cd5-ae15-663614cb6d82 aa5bfec5-5ff6-4de5-b5dc-c1d6dcc6159c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.