d-d sudium bicarbonate u.s.p. bicarbonato de soda puro

Generic: sodium bicarbonate

Labeler: evi labs
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name d-d sudium bicarbonate u.s.p. bicarbonato de soda puro
Generic Name sodium bicarbonate
Labeler evi labs
Dosage Form POWDER
Routes
ORAL
Active Ingredients

sodium bicarbonate 315 mg/g

Manufacturer
Evi Labs

Identifiers & Regulatory

Product NDC 84178-105
Product ID 84178-105_485f9eb1-6536-c47c-e063-6394a90ae32c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2027-12-31
Marketing Start 2026-01-14

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 84178105
Hyphenated Format 84178-105

Supplemental Identifiers

UPC
0748541491085 0748541490040 0748541492167
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 d-d sudium bicarbonate u.s.p. bicarbonato de soda puro (source: ndc)
Generic Name sodium bicarbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 315 mg/g
source: ndc
Packaging
  • 113 g in 1 BOTTLE, PLASTIC (84178-105-02)
  • 227 g in 1 BOTTLE, PLASTIC (84178-105-03)
  • 454 g in 1 BOTTLE, PLASTIC (84178-105-04)
source: ndc

Packages (3)

84178-105-02 113 g in 1 BOTTLE, PLASTIC (84178-105-02) 84178-105-03 227 g in 1 BOTTLE, PLASTIC (84178-105-03) 84178-105-04 454 g in 1 BOTTLE, PLASTIC (84178-105-04)

Ingredients (1)

sodium bicarbonate (315 mg/g)

Linked Drug Pages (1)

D-D SUDIUM BICARBONATE U.S.P. BICARBONATO DE SODA PURO ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "485f9eb1-6536-c47c-e063-6394a90ae32c", "openfda": {"upc": ["0748541491085", "0748541490040", "0748541492167"], "unii": ["8MDF5V39QO"], "spl_set_id": ["485f9eb1-6535-c47c-e063-6394a90ae32c"], "manufacturer_name": ["Evi Labs"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "113 g in 1 BOTTLE, PLASTIC (84178-105-02)", "package_ndc": "84178-105-02", "marketing_start_date": "20260114"}, {"sample": false, "description": "227 g in 1 BOTTLE, PLASTIC (84178-105-03)", "package_ndc": "84178-105-03", "marketing_start_date": "20260114"}, {"sample": false, "description": "454 g in 1 BOTTLE, PLASTIC (84178-105-04)", "package_ndc": "84178-105-04", "marketing_start_date": "20260114"}], "brand_name": "D-D SUDIUM BICARBONATE U.S.P. BICARBONATO DE SODA PURO", "product_id": "84178-105_485f9eb1-6536-c47c-e063-6394a90ae32c", "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": "84178-105", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Evi Labs", "product_type": "HUMAN OTC DRUG", "brand_name_base": "D-D SUDIUM BICARBONATE U.S.P.", "brand_name_suffix": "BICARBONATO DE SODA PURO", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "315 mg/g"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260114", "listing_expiration_date": "20271231"}