NDC 86264-010 - Healers Natural Hot Spot and Itch Relief

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: 86264-010
Package NDCs from labels: 86264-010-04
Manufacturer: Healers PetCare, Inc
Effective date: 2026-06-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Healers Natural Hot Spot and Itch Relief - Healers PetCare, Inc	Healers PetCare, Inc	2026-06-10	OTC ANIMAL DRUG LABEL

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 82 of 82 · 1,624 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pre Post Surgery	HYPERICUM PERFORATUM, SYMPHYTUM OFFICINALE, ARNICA MONTANA	BioActive Nutritional, Inc.	2b20250f-4ca5-49a9-857f-7bef4ec86778	2016-11-10	Warnings	Exact identifier unii: M9VVZ08EKQ
Inflammation II	ASTRAGALUS MEMBRANACEUS, ECHINACEA (ANGUSTIFOLIA), SARSAPARILLA (SMILAX REGELII), TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, THYROIDINUM (SUIS), AURUM METALLICUM, CARBO ANIMALIS, CAUSTICUM, GELSEMIUM SEMPERVIRENS, NATRUM SULPHURICUM, PHOSPHORUS, SULPHUR, THUJA OCCIDENTALIS	BioActive Nutritional, Inc.	4c36e714-f564-41d3-a6b8-60e633defaff	2016-10-04	Warnings	Exact identifier unii: ZW3Z11D0JV
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Eagle Brand Medicated Roll On Refresh	CAMPHOR, MENTHOL	Borden Company (Private) Limited	567b6820-fb52-630e-e063-6294a90a8bf8	2015-07-01	Warnings	Exact identifier unii: AV092KU4JH

Reported adverse events (FAERS/openFDA)#

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