Home NDC 48106-1135-3 NDC 48106-1135-3 - Ice Block This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 48106-1135
Requested NDC 48106-1135-3
Package NDCs from labels 48106-1135-1, 48106-1135-2, 48106-1135-3, 48106-1135-4, 48106-1135-5, 48106-1135-6
Manufacturer BouMatic, LLC
Effective date 2012-01-01
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Ice Block - BouMatic, LLC BouMatic, LLC 2012-01-01 OTC ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48106-1135-1 Ice Block 3.8 L in 1 DRUM LIQUID 3.8 2 48106-1135-2 Ice Block 18.9 L in 1 DRUM LIQUID 18.9 2 48106-1135-3 Ice Block 56.8 L in 1 DRUM LIQUID 56.8 2 48106-1135-4 Ice Block 114 L in 1 DRUM LIQUID 114 2 48106-1135-5 Ice Block 208 L in 1 DRUM LIQUID 208 2 48106-1135-6 Ice Block 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK LIQUID 1040 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48106-1135 ICE BLOCK (SODIUM CAPRYLATE) LIQUID [BOUMATIC, LLC] 2 6 package rows 20120531_fd7162a1-5b9b-4bae-a031-63ee05a84ab5.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.