Home NDC 42829-402 SinuCleanse Neti-Pot
Product NDC 42829-402
11-digit product format 428290402
Labeler code 42829
Product ID 42829-402_2d072944-c4d1-52a1-e063-6394a90a587b
Type HUMAN OTC DRUG
Nonproprietary name SODIUM BICARBONATE, SODIUM CHLORIDE
Dosage form KIT
Route NASAL
Labeler ASCENT CONSUMER PRODUCTS, INC.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2015-02-01
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base SinuCleanse Neti-Pot
Listing expiration 2026-12-31 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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 42829-401-01 SinuCleanse Neti-Pot 3000 mg in 1 PACKET POWDER, FOR SOLUTION 90000 mg 2300 mg in 3000mg 11 42829-402-30 SinuCleanse Neti-Pot 1 in 1 KIT KIT 1 11
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM BICARBONATE ACTIVE INGREDIENT 8MDF5V39QO SINUCLEANSE NETI-POT (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] 2 SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X SINUCLEANSE NETI-POT (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] 2 BICARBONATE ION ACTIVE MOIETY HN1ZRA3Q20 SINUCLEANSE NETI-POT (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] 2 SODIUM CATION ACTIVE MOIETY LYR4M0NH37 SINUCLEANSE NETI-POT (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 42829-402 SINUCLEANSE NETI-POT (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] 11 Current NDC, Legacy NDC, 2 package rows 20250202_ba953a99-4885-4823-9905-75ce3eae160c.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.
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 42829-401-01 42829040101 3000 mg in 1 PACKET 3000 mg Historical 42829-402-30 42829040230 1 KIT in 1 KIT (42829-402-30) * 3000 mg in 1 PACKET (42829-401-01) 1 kit 2015-02-01 0000-00-00 No No Current