FDA.reportPublic FDA data

CVS

Product NDC
69842-453
Requested package NDC
69842-453-10
11-digit product format
698420453
Labeler code
69842
Product ID
69842-453_2d40a1fb-bd05-ccbe-e063-6394a90ad6be
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Chloride, Sodium Bicarbonate
Dosage form
KIT
Labeler
CVS Pharmacy, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-04-24
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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

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
fe2ac0d1-18d4-4cff-833d-5e5eab783352Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
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
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
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
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
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
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
69842-453-102020-06-08C16284748780-19d75b9d0-da3e-f424-e053-dadaa90a57ceCVS Soft Tip Squeeze Sinus Wash System
69842-453-102020-01-31C16284748780-19d75b9d0-da3e-f424-e053-dadaa90a57ceCVS Soft Tip Squeeze Sinus Wash System

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-324-01CVS3000 mg in 1 PACKETPOWDER3000 mg22.8 mg in 100mg7
69842-453-10CVS1 in 1 KITKIT17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-453CVS (SODIUM CHLORIDE, SODIUM BICARBONATE) KIT [CVS PHARMACY, INC.]7Current NDC, Legacy NDC, 2 package rows20250205_fe2ac0d1-18d4-4cff-833d-5e5eab783352.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 CHLORIDE, SODIUM BICARBONATECVS Pharmacy, Inc.fe2ac0d1-18d4-4cff-833d-5e5eab7833522025-02-03WarningsExact identifier
ndc (package): 69842-453-10
ndc (product): 69842-453
ndc11 (package): 69842045310

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionPSNfe2ac0d1-18d4-4cff-833d-5e5eab7833527
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionSCDfe2ac0d1-18d4-4cff-833d-5e5eab7833527
1542919NaHCO3 700 MG / NaCl 2300 MG Powder for Nasal SolutionSYfe2ac0d1-18d4-4cff-833d-5e5eab7833527

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-453-10698420453101 KIT in 1 KIT (69842-453-10) * 30 PACKET in 1 KIT / 3000 mg in 1 PACKET (69842-324-01) 1 kit2017-04-240000-00-00NoNoCurrent