Home NDC 71447-032-00 NDC 71447-032-00 - NELLY DEVUYST BIOSOLAR COLORLIFT 1 TINTED SUNSCREEN 30 mL SPF30 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 71447-032
Requested NDC 71447-032-00
Package NDCs from labels 71447-032-00, 71447-032-01
Manufacturer LABORATOIRES DRUIDE INC
Effective date 2021-04-26
Current FDA listing Not matched in FDA.report NDC product tables FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71447-032-00 NELLY DEVUYST BIOSOLAR COLORLIFT 1 TINTED SUNSCREEN 30 mLSPF30 30 g in 1 TUBE CREAM 30 1 71447-032-01 NELLY DEVUYST BIOSOLAR COLORLIFT 1 TINTED SUNSCREEN 30 mLSPF30 1 in 1 BOX CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71447-032 NELLY DEVUYST BIOSOLAR COLORLIFT 1 TINTED SUNSCREEN 30 ML SPF30 (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [LABORATOIRES DRUIDE INC] 1 Legacy NDC, 2 package rows 20211220_d3824e06-097d-4f23-e053-2a95a90a8cc9.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 37 of 363 · 7,260 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.