CBD Clinic Pain Relief - Level 4

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: CBD Clinic Pain Relief - Level 4
Generic name: MENTHOL, CAMPHOR
Manufacturer: ABACUS HEALTH PRODUCTS, INC.
Product type: HUMAN OTC DRUG
SPL set ID: f0e9ac7c-a840-2e05-e053-2a95a90a33f1
SPL ID: 3239df55-d6f2-c90d-e063-6394a90ab149
Version: 6
Effective date: 2025-04-07
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:13

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		CBD Clinic Pain Relief - Level 4	openfda.brand_name
generic name		MENTHOL, CAMPHOR	openfda.generic_name
manufacturer name		ABACUS HEALTH PRODUCTS, INC.	openfda.manufacturer_name
ndc	package	73096-764-20	openfda.package_ndc
ndc	package	73096-764-44	openfda.package_ndc
ndc	product	73096-764	openfda.product_ndc
ndc11	package	73096076444	derived:openfda.package_ndc
ndc11	package	73096076420	derived:openfda.package_ndc
spl id		3239df55-d6f2-c90d-e063-6394a90ab149	id
spl set id		f0e9ac7c-a840-2e05-e053-2a95a90a33f1	set_id
unii		L7T10EIP3A	openfda.unii
unii		N20HL7Q941	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 • wounds or damaged skin When using this product • avoid contact with eyes or mucous membranes • do not bandage tightly or use with a heating pad Stop use and ask a doctor if • condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days • excessive skin irritation develops If pregnant or breast-feeding ask a health professional before use Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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