NDC 86099-209 - Banixx Lime Sulfur Dip

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
86099-209
Package NDCs from labels
86099-209-16
Manufacturer
Creative Science
Effective date
2025-12-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Banixx Lime Sulfur Dip - Creative ScienceCreative Science2025-12-05OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86099-209-16Banixx Lime Sulfur Dip473.2 g in 1 BOTTLE, PLASTICSOLUTION, CONCENTRATE473.21

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 1 of 1 ยท 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SulfurCLARIFYING DETOX (ACNE TREATMENT) MASKVege Labs LLC303cea30-0502-0cb8-e063-6394a90ac9ed2025-03-13WarningsName fallback
brand name: Sulfur
SulfurSULFURTrue Botanica, LLC6198f81e-c76f-9f38-e053-2a91aa0a52c32023-06-02WarningsName fallback
brand name: Sulfur

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.