FDA.reportPublic FDA data

CVS

Product NDC
59779-408
Requested package NDC
59779-408-01
11-digit product format
597790408
Labeler code
59779
Product ID
59779-408_2d0433c9-8f79-17a1-e063-6394a90acb88
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM BICARBONATE, SODIUM CHLORIDE
Dosage form
POWDER
Route
NASAL
Labeler
CVS Pharmacy
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2013-06-01
Substance
SODIUM BICARBONATE; SODIUM CHLORIDE
Active strength
22.8; 77.8 mg/100mg; mg/100mg
Pharmacologic classes
Alkalinizing Activity [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage59779-40859779-408-01IInactivated by FDAexcluded / ndc_excluded.zip1332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
CVS
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM BICARBONATE22.8 mg/100mg
SODIUM CHLORIDE77.8 mg/100mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8MDF5V39QOInternal UNII lookup
451W47IQ8XInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1542919Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
bccefef8-f92d-42fc-90fc-86644d1df655Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
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
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
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
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct 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
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, Indexing SPL table
NDCEffectiveIndexing SPLRelated label
59779-408-012024-03-089d75b9d0-073f-f424-e053-dadaa90a57ceCVS
59779-408-022024-03-089d75b9d0-073f-f424-e053-dadaa90a57ceCVS
59779-408-012024-01-309d75b9d0-073f-f424-e053-dadaa90a57ceCVS
59779-408-022024-01-309d75b9d0-073f-f424-e053-dadaa90a57ceCVS
59779-408-012021-12-269d75b9d0-073f-f424-e053-dadaa90a57ceCVS
59779-408-022021-12-269d75b9d0-073f-f424-e053-dadaa90a57ceCVS
59779-408-012021-07-239d75b9d0-073f-f424-e053-dadaa90a57ceCVS
59779-408-022021-07-239d75b9d0-073f-f424-e053-dadaa90a57ceCVS
59779-408-012020-02-039d75b9d0-073f-f424-e053-dadaa90a57ceCVS
59779-408-002020-01-319d75b9d0-2f8f-f424-e053-dadaa90a57ceDrug Facts
59779-408-012020-01-319d75b9d0-073f-f424-e053-dadaa90a57ceCVS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59779-408-01CVS3000 mg in 1 PACKETPOWDER300010
59779-408-02CVS1 in 1 BOXPOWDER110
59779-408-02CVS3000 mg in 1 PACKETPOWDER300010
59779-408-00Refill Saline Packets1 in 1 PACKETPOWDER, FOR SOLUTION17
59779-408-00Refill Saline Packets100 in 1 CARTONPOWDER, FOR SOLUTION1007
59779-408-01CVS3000 mg in 1 PACKETPOWDER3000 mg77.8 mg in 100mg4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM BICARBONATEACTIVE INGREDIENT8MDF5V39QOREFILL SALINE PACKETS (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [CVS PHARMACY]7
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8XREFILL SALINE PACKETS (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [CVS PHARMACY]7
BICARBONATE IONACTIVE MOIETYHN1ZRA3Q20REFILL SALINE PACKETS (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [CVS PHARMACY]7
SODIUM CATIONACTIVE MOIETYLYR4M0NH37REFILL SALINE PACKETS (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [CVS PHARMACY]7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59779-408CVS (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER [CVS PHARMACY]10Current NDC, Legacy NDC, 3 package rows20250202_bccefef8-f92d-42fc-90fc-86644d1df655.zip
59779-408REFILL SALINE PACKETS (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [CVS PHARMACY]7Current NDC, Legacy NDC, 2 package rows20130604_d7e58c98-102d-4ae5-9af0-c9f38a0c18b6.zip
59779-408CVS (SODIUM CHLORIDE, SODIUM BICARBONATE) KIT [CVS PHARMACY]4Current NDC, Legacy NDC20160325_dcbdb1cb-19fa-45bf-91c8-a984b32dcfa6.zip
59779-408CVS (SODIUM CHLORIDE, SODIUM BICARBONATE) KIT [CVS PHARMACY]2Current NDC, Legacy NDC20161205_ad8ac605-579e-4ade-975e-dc9a796b3942.zip
59779-408CVS (SODIUM CHLORIDE, SODIUM BICARBONATE) KIT [CVS PHARMACY]2Current NDC, Legacy NDC20170115_ab873baf-97b8-45fd-ab5d-6edd068e3e8f.zip

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
CVSSODIUM BICARBONATE, SODIUM CHLORIDECVS Pharmacybccefef8-f92d-42fc-90fc-86644d1df6552025-01-31WarningsExact identifier
ndc (package): 59779-408-01
ndc (product): 59779-408
ndc11 (package): 59779040801

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionPSNbccefef8-f92d-42fc-90fc-86644d1df65510
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionSCDbccefef8-f92d-42fc-90fc-86644d1df65510
1542919NaHCO3 700 MG / NaCl 2300 MG Powder for Nasal SolutionSYbccefef8-f92d-42fc-90fc-86644d1df65510
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionPSNdcbdb1cb-19fa-45bf-91c8-a984b32dcfa64
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionSCDdcbdb1cb-19fa-45bf-91c8-a984b32dcfa64
1542919NaHCO3 700 MG / NaCl 2300 MG Powder for Nasal SolutionSYdcbdb1cb-19fa-45bf-91c8-a984b32dcfa64

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59779-408-01597790408013000 mg in 1 PACKET (59779-408-01) 3000 mg2013-06-010000-00-00NoNoCurrent