BOA VIDA Antifungal

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: BOA VIDA Antifungal
Generic name: MICONAZOLE NITRATE
Manufacturer: Central Solutions Inc
Product type: HUMAN OTC DRUG
SPL set ID: 69c5340d-9abd-43bf-a90b-9568d615f06f
SPL ID: 28d9ee71-5798-8236-e063-6294a90adbd4
Version: 3
Effective date: 2024-12-09
Source export date: 2026-10-27
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:13:04

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		BOA VIDA Antifungal	openfda.brand_name
generic name		MICONAZOLE NITRATE	openfda.generic_name
manufacturer name		Central Solutions Inc	openfda.manufacturer_name
ndc	package	62654-147-01	openfda.package_ndc
ndc	product	62654-147	openfda.product_ndc
ndc11	package	62654014701	derived:openfda.package_ndc
rxcui		998483	openfda.rxcui
spl id		28d9ee71-5798-8236-e063-6294a90adbd4	id
spl set id		69c5340d-9abd-43bf-a90b-9568d615f06f	set_id
unii		VW4H1CYW1K	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use on children under 2 years of age for diaper rash. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If irritation occurs or if there is no improvement withing 4 weeks for athlete's foot or ringworm, or within 2 weeks for jock itch, discontinue use and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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