de la cruz sodium bicarbonate antacid

Generic: sodium bicarbonate

Labeler: dlc laboratories, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name de la cruz sodium bicarbonate antacid
Generic Name sodium bicarbonate
Labeler dlc laboratories, inc.
Dosage Form POWDER
Routes
ORAL
Active Ingredients

sodium bicarbonate 2.6 g/2.6g

Manufacturer
DLC Laboratories, Inc.

Identifiers & Regulatory

Product NDC 24286-1537
Product ID 24286-1537_47d4f7e8-3e03-1192-e063-6294a90aa739
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2027-12-31
Marketing Start 2013-09-25

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 242861537
Hyphenated Format 24286-1537

Supplemental Identifiers

RxCUI
1488624
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 de la cruz sodium bicarbonate antacid (source: ndc)
Generic Name sodium bicarbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.6 g/2.6g
source: ndc
Packaging
  • 113 g in 1 BOTTLE, PLASTIC (24286-1537-7)
  • 226 g in 1 BOTTLE, PLASTIC (24286-1537-8)
source: ndc

Packages (2)

24286-1537-7 113 g in 1 BOTTLE, PLASTIC (24286-1537-7) 24286-1537-8 226 g in 1 BOTTLE, PLASTIC (24286-1537-8)

Ingredients (1)

sodium bicarbonate (2.6 g/2.6g)

Linked Drug Pages (1)

DE LA CRUZ SODIUM BICARBONATE ANTACID ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47d4f7e8-3e03-1192-e063-6294a90aa739", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1488624"], "spl_set_id": ["fc469943-9749-45ee-93f7-90fdbcdc7215"], "manufacturer_name": ["DLC Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "113 g in 1 BOTTLE, PLASTIC (24286-1537-7)", "package_ndc": "24286-1537-7", "marketing_start_date": "20130925"}, {"sample": false, "description": "226 g in 1 BOTTLE, PLASTIC (24286-1537-8)", "package_ndc": "24286-1537-8", "marketing_start_date": "20190722"}], "brand_name": "DE LA CRUZ SODIUM BICARBONATE ANTACID", "product_id": "24286-1537_47d4f7e8-3e03-1192-e063-6294a90aa739", "dosage_form": "POWDER", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "24286-1537", "generic_name": "SODIUM BICARBONATE", "labeler_name": "DLC Laboratories, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DE LA CRUZ SODIUM BICARBONATE ANTACID", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "2.6 g/2.6g"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130925", "listing_expiration_date": "20271231"}