sinucleanse

Generic: sodium bicarbonate, sodium chloride

Labeler: ascent consumer products, inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name sinucleanse
Generic Name sodium bicarbonate, sodium chloride
Labeler ascent consumer products, inc.
Dosage Form POWDER, FOR SOLUTION
Routes
NASAL
Active Ingredients

sodium bicarbonate 700 mg/3000mg, sodium chloride 2300 mg/3000mg

Manufacturer
ASCENT CONSUMER PRODUCTS, INC.

Identifiers & Regulatory

Product NDC 42829-401
Product ID 42829-401_2d073cca-7bcc-d1bd-e063-6294a90a0c39
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2015-02-01

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42829401
Hyphenated Format 42829-401

Supplemental Identifiers

RxCUI
1542919
UNII
8MDF5V39QO 451W47IQ8X

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sinucleanse (source: ndc)
Generic Name sodium bicarbonate, sodium chloride (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 700 mg/3000mg
  • 2300 mg/3000mg
source: ndc
Packaging
  • 3000 mg in 1 PACKET (42829-401-01)
source: ndc

Packages (1)

42829-401-01 3000 mg in 1 PACKET (42829-401-01)

Ingredients (2)

sodium bicarbonate (700 mg/3000mg) sodium chloride (2300 mg/3000mg)

Linked Drug Pages (1)

SinuCleanse ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "2d073cca-7bcc-d1bd-e063-6294a90a0c39", "openfda": {"unii": ["8MDF5V39QO", "451W47IQ8X"], "rxcui": ["1542919"], "spl_set_id": ["c33bf872-54aa-45e0-9e40-a6565a13f198"], "manufacturer_name": ["ASCENT CONSUMER PRODUCTS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3000 mg in 1 PACKET (42829-401-01)", "package_ndc": "42829-401-01", "marketing_start_date": "20150201"}], "brand_name": "SinuCleanse", "product_id": "42829-401_2d073cca-7bcc-d1bd-e063-6294a90a0c39", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["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]"], "product_ndc": "42829-401", "generic_name": "SODIUM BICARBONATE, SODIUM CHLORIDE", "labeler_name": "ASCENT CONSUMER PRODUCTS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SinuCleanse", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "700 mg/3000mg"}, {"name": "SODIUM CHLORIDE", "strength": "2300 mg/3000mg"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20150201", "listing_expiration_date": "20261231"}