Home NDC 72636-101-01 NDC 72636-101-01 - Perilla Fo ti Conditioner 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 72636-101
Requested NDC 72636-101-01
Package NDCs from labels 72636-101-01, 72636-101-02
Manufacturer The Greenery Lab | Evercos Co., Ltd.
Effective date 2018-11-13
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Perilla Fo-ti Conditioner The Greenery Lab | Evercos Co., Ltd. 2018-11-13 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 72636-101-01 Perilla Fo ti Conditioner 500 g in 1 BOTTLE, PUMP SOLUTION 500 3 72636-101-02 Perilla Fo ti Conditioner 1 in 1 BOX SOLUTION 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72636-101 PERILLA FO TI CONDITIONER (MENTHOL, SALICYLIC ACID, PANTHENOL) SOLUTION [THE GREENERY LAB] 3 Legacy NDC, 2 package rows 20181114_798c853c-16a5-8502-e053-2a91aa0a6532.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 151 of 191 · 3,813 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.