Home NDC 0132-0190 Pedia-Lax
Product NDC 0132-0190
11-digit product format 001320190
Labeler code 0132
Product ID 0132-0190_530334c7-fa4f-462f-8816-5ad794056ef4
Type HUMAN OTC DRUG
Nonproprietary name Glycerin
Dosage form LIQUID
Route RECTAL
Labeler C.B. Fleet Company, Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2008-03-01
Substance GLYCERIN
Active strength 2.8 g/2.7mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0132-0190 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 0132-0190 0132-0190-12 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GLYCERIN 2.8 g/2.7mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination PDC6A3C0OX Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 895966 Internal RxNorm lookup 1190433 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0132-0190-12 Pedia-Lax 4 mL in 1 APPLICATOR LIQUID 4 11 0132-0190-12 Pedia-Lax 6 in 1 CARTON LIQUID 6 11
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0132-0190 PEDIA-LAX (GLYCERIN) LIQUID [C.B. FLEET COMPANY, INC.] 11 Current NDC, Legacy NDC, 2 package rows 20250119_4e15f6ca-a40c-485f-be3f-07c2ed7cb498.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 30 of 42 · 833 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 0132-0190-12 00132019012 6 APPLICATOR in 1 CARTON (0132-0190-12) / 4 mL in 1 APPLICATOR 6 applicator 2008-03-01 0000-00-00 No No Current