SinuCleanse

Product NDC
42829-408
11-digit product format
428290408
Labeler code
42829
Product ID
42829-408_2d03e738-ae54-175c-e063-6394a90aed10
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM BICARBONATE, SODIUM CHLORIDE
Dosage form
POWDER, FOR SOLUTION
Route
NASAL
Labeler
ASCENT CONSUMER PRODUCTS, INC.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2015-02-01
Substance
SODIUM BICARBONATE; SODIUM CHLORIDE
Active strength
22.2; 77.8 mg/100mg; mg/100mg
Pharmacologic classes
Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM BICARBONATE22.2 mg/100mg
SODIUM CHLORIDE77.8 mg/100mg

Harmonized Identifiers#

Field, Values table
FieldValues
Unii8MDF5V39QO, 451W47IQ8X
Rxcui1542919

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
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
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, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42829-408-602025-12-10C16284748780-13b156c62-2ed4-fb37-e063-e6dba90a4e07SinuCleanse
42829-408-602025-07-29C16284748780-13b156c62-2ed4-fb37-e063-e6dba90a4e07SinuCleanse

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42829-408-00SinuCleanse3000 mg in 1 PACKETPOWDER, FOR SOLUTION30009
42829-408-00SinuCleanse100 in 1 CARTONPOWDER, FOR SOLUTION1009
42829-408-60SinuCleanse60 in 1 CARTONPOWDER, FOR SOLUTION609
42829-408-60SinuCleanse3000 mg in 1 PACKETPOWDER, FOR SOLUTION30009

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42829-408SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.]9Current NDC, Legacy NDC, 2 package rows20250201_ff4df6c5-c85f-406a-89d7-8c2853fd5e10.zip
42829-408SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.]8Current NDC, Legacy NDC, 2 package rows20210222_beb842fa-2373-4f21-9631-ef20ee124584.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionPSNbeb842fa-2373-4f21-9631-ef20ee1245849
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionPSNff4df6c5-c85f-406a-89d7-8c2853fd5e109
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionSCDbeb842fa-2373-4f21-9631-ef20ee1245849
1542919sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal SolutionSCDff4df6c5-c85f-406a-89d7-8c2853fd5e109
1542919NaHCO3 700 MG / NaCl 2300 MG Powder for Nasal SolutionSYbeb842fa-2373-4f21-9631-ef20ee1245849
1542919NaHCO3 700 MG / NaCl 2300 MG Powder for Nasal SolutionSYff4df6c5-c85f-406a-89d7-8c2853fd5e109

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42829-408-0042829040800100 PACKET in 1 CARTON (42829-408-00) / 3000 mg in 1 PACKET100 packet2015-12-010000-00-00NoNoCurrent
42829-408-604282904086060 PACKET in 1 CARTON (42829-408-60) / 3000 mg in 1 PACKET60 packet2015-02-010000-00-00NoNoCurrent