Home NDC 51706-113-01 NDC 51706-113-01 - Bodycology Brown Sugar Vanilla 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 51706-113
Requested NDC 51706-113-01
Package NDCs from labels 51706-113-01, 51706-113-02
Manufacturer Landy International | Wal-Mart Stores, Inc.
Effective date 2010-06-24
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Brown Sugar Vanilla Landy International | Wal-Mart Stores, Inc. 2010-06-24 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51706-113-01 BodycologyBrown Sugar Vanilla 177 mL in 1 BOTTLE GEL 177 3 51706-113-02 BodycologyBrown Sugar Vanilla 1 in 1 KIT GEL 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51706-113 BODYCOLOGY BROWN SUGAR VANILLA (TRICLOSAN) GEL [LANDY INTERNATIONAL] 3 Legacy NDC, 2 package rows 20100625_d2aaa375-1fa8-4172-b472-e77a08a0844b.zip
DailyMed Socrata Ingredients# 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 1 of 1 ยท 12 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.