Home NDC 70969-101-01 NDC 70969-101-01 - Ginseng Whitening 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 70969-101
Requested NDC 70969-101-01
Package NDCs from labels 70969-101-01, 70969-101-02
Manufacturer Synbio Co., Ltd.
Effective date 2016-09-19
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Ginseng Whitening Cream Synbio Co., Ltd. 2016-09-19 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 70969-101-01 Ginseng Whitening 50 g in 1 CONTAINER CREAM 50 1 70969-101-02 Ginseng Whitening 1 in 1 PACKAGE CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70969-101 GINSENG WHITENING (NIACINAMIDE) CREAM [SYNBIO CO., LTD.] 1 Legacy NDC, 2 package rows 20160920_53f5af8c-9d88-4e89-97b2-6460d18d6fee.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 13 of 72 · 1,430 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.