pedia-lax

Generic: magnesium hydroxide

Labeler: c.b. fleet company, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pedia-lax
Generic Name magnesium hydroxide
Labeler c.b. fleet company, inc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

magnesium hydroxide 400 mg/1

Manufacturer
C.B. Fleet Company, Inc.

Identifiers & Regulatory

Product NDC 0132-0655
Product ID 0132-0655_ba6860a3-95dd-4ab8-8c1d-95aa836443f1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2008-03-01

Pharmacologic Class

Classes
calculi dissolution agent [epc] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] inhibition small intestine fluid/electrolyte absorption [pe] magnesium ion exchange activity [moa] osmotic activity [moa] osmotic laxative [epc] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01320655
Hyphenated Format 0132-0655

Supplemental Identifiers

RxCUI
790436 1088243
UNII
NBZ3QY004S

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 pedia-lax (source: ndc)
Generic Name magnesium hydroxide (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0132-0655-01) / 30 TABLET, CHEWABLE in 1 BOTTLE
source: ndc

Packages (1)

0132-0655-01 1 BOTTLE in 1 CARTON (0132-0655-01) / 30 TABLET, CHEWABLE in 1 BOTTLE

Ingredients (1)

magnesium hydroxide (400 mg/1)

Linked Drug Pages (1)

Pedia-Lax ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ba6860a3-95dd-4ab8-8c1d-95aa836443f1", "openfda": {"unii": ["NBZ3QY004S"], "rxcui": ["790436", "1088243"], "spl_set_id": ["975f24d8-218c-40f4-84a5-558acf34329d"], "manufacturer_name": ["C.B. Fleet Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0132-0655-01)  / 30 TABLET, CHEWABLE in 1 BOTTLE", "package_ndc": "0132-0655-01", "marketing_start_date": "20080301"}], "brand_name": "Pedia-Lax", "product_id": "0132-0655_ba6860a3-95dd-4ab8-8c1d-95aa836443f1", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "0132-0655", "generic_name": "Magnesium hydroxide", "labeler_name": "C.B. Fleet Company, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pedia-Lax", "active_ingredients": [{"name": "MAGNESIUM HYDROXIDE", "strength": "400 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20080301", "listing_expiration_date": "20261231"}