Home NDC 81817-101-01 NDC 81817-101-01 - ZENOTRI Scalp Essence 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 81817-101
Requested NDC 81817-101-01
Package NDCs from labels 81817-101-01, 81817-101-03, 81817-101-02
Manufacturer CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD
Effective date 2021-05-13
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type ZENOTRI Scalp Essence - CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD 2021-05-13 HUMAN OTC DRUG LABEL ZENOTRI Scalp Essence - CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD 2021-04-22 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 81817-101-01 ZENOTRI Scalp Essence 25 mL in 1 TUBE GEL 25 3 81817-101-03 ZENOTRI Scalp Essence 1 in 1 CARTON GEL 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81817-101 ZENOTRI SCALP ESSENCE (SALICYLIC ACID) GEL [CHROMACH CO., LTD.] 3 Legacy NDC, 2 package rows 20210514_c231cbcd-4fe5-16ba-e053-2a95a90a2f8d.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 33 of 204 · 4,073 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.