FDA.reportPublic FDA data

Saline Nasal Spray

Manufacturer
Velocity Pharma LLC
Effective date
2019-11-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:01:33

Label at a glance#

ProductSaline Nasal 1.5oz
Active ingredientSODIUM CHLORIDE
Label structure7 sections

Indications and uses

For dry nasal membranes

Dosage and administration

Squeeze twice in each nostril as needed Upright delivers a spray, horizontally a stream, upside down a drop

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride, 0.65%

Purpose

OTC - PURPOSE SECTION

Moisturizer

Uses

INDICATIONS & USAGE SECTION

For dry nasal membranes

Warnings

WARNINGS SECTION

Do not use if seal is broken or missing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. The use of this dispenser by more than one person may spread infection.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Squeeze twice in each nostril as needed
  • Upright delivers a spray, horizontally a stream, upside down a drop

Inactive ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium chloride, Disodium phosphate, Phenylcarbinol, Monosodium phosphate, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SalineSaline

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
707251sodium chloride 0.65 % Nasal SprayPSN2
707251sodium chloride 6.5 MG/ML Nasal SpraySCD2
707251NaCl 6.5 MG/ML Nasal SpraySY2
707251sodium chloride 0.65 % Nasal SpraySY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76168-602-152021-01-29C16284748780-1ba0f9c33-490b-a910-e053-dadaa90a0b85Saline Nasal Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76168-602-15Saline Nasal1.5oz44 mL in 1 BOTTLE, SPRAYSPRAY442

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76168-602SALINE NASAL 1.5OZ (SODIUM CHLORIDE 0.65%) SPRAY [VELOCITY PHARMA LLC]2Legacy NDC, 1 package rows20191120_06d66a1c-18ea-456b-a400-9666d374a615.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76168-60276168-602-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS22ADO53M6FIACT
BENZYL ALCOHOLLKG8494WBHIACT
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUSKH7I04HPUUIACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XACTIB

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
97b51448-81d7-5817-e053-2995a90af43f06d66a1c-18ea-456b-a400-9666d374a6152019-11-19WarningsExact identifier
spl id: 97b51448-81d7-5817-e053-2995a90af43f
spl set id: 06d66a1c-18ea-456b-a400-9666d374a615

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.