Naturasil Cherry Angiomas

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: Naturasil Cherry Angiomas
Generic name: PHOSPHORICUM ACIDUM
Manufacturer: Nature's Innovation
Product type: HUMAN OTC DRUG
SPL set ID: b512f00e-7b3e-4c7b-a0e6-ebffd84b231f
SPL ID: 302fc1b1-e4a6-4b73-a485-d7d423a8eec9
Version: 3
Effective date: 2021-01-14
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:17:13

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Naturasil Cherry Angiomas	openfda.brand_name
generic name		PHOSPHORICUM ACIDUM	openfda.generic_name
manufacturer name		Nature's Innovation	openfda.manufacturer_name
ndc	package	10893-120-10	openfda.package_ndc
ndc	product	10893-120	openfda.product_ndc
ndc11	package	10893012010	derived:openfda.package_ndc
spl id		302fc1b1-e4a6-4b73-a485-d7d423a8eec9	id
spl set id		b512f00e-7b3e-4c7b-a0e6-ebffd84b231f	set_id
unii		E4GA8884NN	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 . Ask a doctor before use if pregnant or nursing. Don't apply to eye or eye area. Keep out of reach of children. Do not use if tamper evident seal is broken. In case of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.

Reported adverse events (FAERS/openFDA)#

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