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 22.2 mg/100mg, sodium chloride 77.8 mg/100mg

Manufacturer
ASCENT CONSUMER PRODUCTS, INC.

Identifiers & Regulatory

Product NDC 42829-408
Product ID 42829-408_459b6035-e645-208a-e063-6294a90aef87
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 42829408
Hyphenated Format 42829-408

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
  • 22.2 mg/100mg
  • 77.8 mg/100mg
source: ndc
Packaging
  • 60 PACKET in 1 CARTON (42829-408-60) / 3000 mg in 1 PACKET
source: ndc

Packages (1)

Ingredients (2)

sodium bicarbonate (22.2 mg/100mg) sodium chloride (77.8 mg/100mg)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "459b6035-e645-208a-e063-6294a90aef87", "openfda": {"unii": ["8MDF5V39QO", "451W47IQ8X"], "rxcui": ["1542919"], "spl_set_id": ["beb842fa-2373-4f21-9631-ef20ee124584"], "manufacturer_name": ["ASCENT CONSUMER PRODUCTS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 PACKET in 1 CARTON (42829-408-60)  / 3000 mg in 1 PACKET", "package_ndc": "42829-408-60", "marketing_start_date": "20150201"}], "brand_name": "SinuCleanse", "product_id": "42829-408_459b6035-e645-208a-e063-6294a90aef87", "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": "42829-408", "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": "22.2 mg/100mg"}, {"name": "SODIUM CHLORIDE", "strength": "77.8 mg/100mg"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20150201", "listing_expiration_date": "20261231"}