PM Recovery Pain Relief

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: PM Recovery Pain Relief
Generic name: CAMPHOR, MENTHOL
Manufacturer: Charlotte's Web, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 3aa08859-809d-de8c-e063-6394a90a8e25
SPL ID: 3aa08859-809e-de8c-e063-6394a90a8e25
Version: 1
Effective date: 2025-08-01
Source export date: 2026-11-06
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/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:48:56

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		PM Recovery Pain Relief	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		Charlotte's Web, Inc.	openfda.manufacturer_name
ndc	package	79845-770-30	openfda.package_ndc
ndc	product	79845-770	openfda.product_ndc
ndc11	package	79845077030	derived:openfda.package_ndc
rxcui		2720403	openfda.rxcui
spl id		3aa08859-809e-de8c-e063-6394a90a8e25	id
spl set id		3aa08859-809d-de8c-e063-6394a90a8e25	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 When using this product avoid contact with eyes, nostrils and mouth do not apply to wounds or damaged skin do not bandage tightly 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 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.