Home NDC 42829-408-60 SinuCleanse
Product NDC 42829-408
Requested package NDC 42829-408-60
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 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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 42829-408 42829-408-60 I Inactivated by FDA excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 42829-408 42829-408-60 I Inactivated by FDA excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Additional Listing Data#
Finished product Yes
Brand name base SinuCleanse
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BICARBONATE 22.2 mg/100mg SODIUM CHLORIDE 77.8 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8MDF5V39QO Internal UNII lookup 451W47IQ8X Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1542919 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 42829-408-00 SinuCleanse 3000 mg in 1 PACKET POWDER, FOR SOLUTION 3000 9 42829-408-00 SinuCleanse 100 in 1 CARTON POWDER, FOR SOLUTION 100 9 42829-408-60 SinuCleanse 60 in 1 CARTON POWDER, FOR SOLUTION 60 9 42829-408-60 SinuCleanse 3000 mg in 1 PACKET POWDER, FOR SOLUTION 3000 9
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM BICARBONATE ACTIVE INGREDIENT 8MDF5V39QO SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 4 SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 4 BICARBONATE ION ACTIVE MOIETY HN1ZRA3Q20 SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 4 SODIUM CATION ACTIVE MOIETY LYR4M0NH37 SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 4 SODIUM BICARBONATE ACTIVE INGREDIENT 8MDF5V39QO SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 2 SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 2 BICARBONATE ION ACTIVE MOIETY HN1ZRA3Q20 SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 2 SODIUM CATION ACTIVE MOIETY LYR4M0NH37 SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 42829-408 SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 9 Current NDC, Legacy NDC, 2 package rows 20250201_ff4df6c5-c85f-406a-89d7-8c2853fd5e10.zip 42829-408 SINUCLEANSE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [ASCENT CONSUMER PRODUCTS, INC.] 8 Current NDC, Legacy NDC, 2 package rows 20210222_beb842fa-2373-4f21-9631-ef20ee124584.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 · 2 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 42829-408-60 42829040860 60 PACKET in 1 CARTON (42829-408-60) / 3000 mg in 1 PACKET 60 packet 2015-02-01 0000-00-00 No No Current