Home NDC 70381-112-01 NDC 70381-112-01 - Acne Control Clarifying Body Spry 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 70381-112
Requested NDC 70381-112-01
Package NDCs from labels 70381-112-01, 70381-112-02
Manufacturer Murad, LLC | Cosway Company, Inc.
Effective date 2021-07-02
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Acne Control Clarifying Body Spray Murad, LLC | Cosway Company, Inc. 2021-07-02 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 70381-112-01 Acne Control Clarifying Body Spry 130 mL in 1 BOTTLE SPRAY 130 4 70381-112-02 Acne Control Clarifying Body Spry 1 in 1 CARTON SPRAY 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70381-112 ACNE CONTROL CLARIFYING BODY SPRY (SALICYLIC ACID) SPRAY [MURAD, LLC] 4 Legacy NDC, 2 package rows 20210808_ff4b1797-6c47-4b39-8a48-218cc8524e1f.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 50 of 359 · 7,179 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.