humco sodium bicarbonate

Generic: sodium bicarbonate

Labeler: humco holding group, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name humco sodium bicarbonate
Generic Name sodium bicarbonate
Labeler humco holding group, inc.
Dosage Form POWDER
Routes
ORAL
Active Ingredients

sodium bicarbonate 1000 mg/g

Manufacturer
Humco Holding Group, Inc.

Identifiers & Regulatory

Product NDC 0395-2685
Product ID 0395-2685_45b126e8-c32f-40bc-e063-6294a90a404a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 1998-03-25

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 03952685
Hyphenated Format 0395-2685

Supplemental Identifiers

RxCUI
1110802
UPC
0303952685944 0303952685012
UNII
8MDF5V39QO

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 humco sodium bicarbonate (source: ndc)
Generic Name sodium bicarbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/g
source: ndc
Packaging
  • 454 g in 1 BOTTLE, PLASTIC (0395-2685-01)
  • 113 g in 1 BOTTLE, PLASTIC (0395-2685-94)
source: ndc

Packages (2)

0395-2685-01 454 g in 1 BOTTLE, PLASTIC (0395-2685-01) 0395-2685-94 113 g in 1 BOTTLE, PLASTIC (0395-2685-94)

Ingredients (1)

sodium bicarbonate (1000 mg/g)

Linked Drug Pages (1)

Humco Sodium Bicarbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45b126e8-c32f-40bc-e063-6294a90a404a", "openfda": {"upc": ["0303952685944", "0303952685012"], "unii": ["8MDF5V39QO"], "rxcui": ["1110802"], "spl_set_id": ["aeaa34f6-216d-49f3-8393-c7bda96a3e32"], "manufacturer_name": ["Humco Holding Group, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "454 g in 1 BOTTLE, PLASTIC (0395-2685-01)", "package_ndc": "0395-2685-01", "marketing_start_date": "20171114"}, {"sample": false, "description": "113 g in 1 BOTTLE, PLASTIC (0395-2685-94)", "package_ndc": "0395-2685-94", "marketing_start_date": "20171114"}], "brand_name": "Humco Sodium Bicarbonate", "product_id": "0395-2685_45b126e8-c32f-40bc-e063-6294a90a404a", "dosage_form": "POWDER", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0395-2685", "generic_name": "Sodium Bicarbonate", "labeler_name": "Humco Holding Group, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Humco Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "1000 mg/g"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19980325", "listing_expiration_date": "20261231"}