Hemp Magic Fast-Acting Pain Relief Cream

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: Hemp Magic Fast-Acting Pain Relief Cream
Generic name: MENTHOL
Manufacturer: Nexxus Capital LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4af69640-1413-868b-e063-6394a90a3989
SPL ID: 4af69640-1414-868b-e063-6394a90a3989
Version: 1
Effective date: 2026-02-16
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:06:16

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Hemp Magic Fast-Acting Pain Relief Cream	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Nexxus Capital LLC	openfda.manufacturer_name
ndc	package	85294-001-01	openfda.package_ndc
ndc	package	85294-001-03	openfda.package_ndc
ndc	package	85294-001-04	openfda.package_ndc
ndc	package	85294-001-02	openfda.package_ndc
ndc	product	85294-001	openfda.product_ndc
ndc11	package	85294000104	derived:openfda.package_ndc
ndc11	package	85294000101	derived:openfda.package_ndc
ndc11	package	85294000102	derived:openfda.package_ndc
ndc11	package	85294000103	derived:openfda.package_ndc
spl id		4af69640-1414-868b-e063-6394a90a3989	id
spl set id		4af69640-1413-868b-e063-6394a90a3989	set_id
unii		L7T10EIP3A	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. Avoid contact with eyes Flammable: keep away from fire or flame - use only as directed - do not bandage tightly or use with heating pad - do not apply to wounds or damaged skin Stop use and ask doctor if - condition persist for more than 7 days or worsen, symptoms clear up and occur again within a few days - redness is present - excessive irritation of the skin develops If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Reported adverse events (FAERS/openFDA)#

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