well at walgreens

Generic: sodium bicarbonate, sodium chloride

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name well at walgreens
Generic Name sodium bicarbonate, sodium chloride
Labeler walgreen company
Dosage Form POWDER, FOR SOLUTION
Routes
NASAL
Active Ingredients

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

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-0802
Product ID 0363-0802_2d071d79-fd0e-7b3a-e063-6394a90a04f0
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2013-04-01

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 03630802
Hyphenated Format 0363-0802

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 well at walgreens (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 (0363-0802-00)
source: ndc

Packages (1)

0363-0802-00 3000 mg in 1 PACKET (0363-0802-00)

Ingredients (2)

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

Linked Drug Pages (1)

Well at Walgreens ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "2d071d79-fd0e-7b3a-e063-6394a90a04f0", "openfda": {"unii": ["8MDF5V39QO", "451W47IQ8X"], "rxcui": ["1542919"], "spl_set_id": ["bcd336b4-9189-44d5-ae6d-81e535eff6b5"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3000 mg in 1 PACKET (0363-0802-00)", "package_ndc": "0363-0802-00", "marketing_start_date": "20130401"}], "brand_name": "Well at Walgreens", "product_id": "0363-0802_2d071d79-fd0e-7b3a-e063-6394a90a04f0", "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": "0363-0802", "generic_name": "SODIUM BICARBONATE, SODIUM CHLORIDE", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Well at Walgreens", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "700 mg/3000mg"}, {"name": "SODIUM CHLORIDE", "strength": "2300 mg/3000mg"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20130401", "listing_expiration_date": "20261231"}