NDC 83865-001 - AHA BHA GLOW TONIC

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
83865-001
Package NDCs from labels
83865-001-01
Manufacturer
Skinkure
Effective date
2024-02-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
AHA BHA GLOW TONIC - SkinkureSkinkure2024-02-06HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83865-001-01AHA BHA GLOW TONIC1 in 1 CARTONLIQUID11
83865-001-01AHA BHA GLOW TONIC50 mL in 1 BOTTLE, SPRAYLIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83865-001AHA BHA GLOW TONIC (SALICYLIC ACID) LIQUID [SKINKURE]12 package rows20240214_252bcb52-059a-4476-8b49-436a6155e4df.zip