Home NDC 0132-0655 Pedia-Lax
Product NDC 0132-0655
11-digit product format 001320655
Labeler code 0132
Product ID 0132-0655_ba6860a3-95dd-4ab8-8c1d-95aa836443f1
Type HUMAN OTC DRUG
Nonproprietary name Magnesium hydroxide
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler C.B. Fleet Company, Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2008-03-01
Substance MAGNESIUM HYDROXIDE
Active strength 400 mg/1
Pharmacologic 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]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Pedia-Lax
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM HYDROXIDE 400 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination NBZ3QY004S Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 790436 Internal RxNorm lookup 1088243 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0132-0655-01 Pedia-Lax 30 in 1 BOTTLE TABLET, CHEWABLE 30 7 0132-0655-01 Pedia-Lax 1 in 1 CARTON TABLET, CHEWABLE 1 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Magnesium Hydroxide ACTIVE INGREDIENT NBZ3QY004S PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 Magnesium Hydroxide ACTIVE MOIETY NBZ3QY004S PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 ALUMINUM OXIDE INACTIVE INGREDIENT LMI26O6933 PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 MANNITOL INACTIVE INGREDIENT 3OWL53L36A PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 SORBITOL INACTIVE INGREDIENT 506T60A25R PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 SUCRALOSE INACTIVE INGREDIENT 96K6UQ3ZD4 PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4 WATERMELON INACTIVE INGREDIENT 231473QB6R PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0132-0655 PEDIA-LAX (MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [C.B. FLEET COMPANY, INC.] 7 Current NDC, Legacy NDC, 2 package rows 20240410_975f24d8-218c-40f4-84a5-558acf34329d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 14 of 43 · 858 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0132-0655-01 00132065501 1 BOTTLE in 1 CARTON (0132-0655-01) / 30 TABLET, CHEWABLE in 1 BOTTLE 1 bottle 2008-03-01 0000-00-00 No No Current