PM Recovery Pain Relief

Manufacturer
Charlotte's Web, Inc. | Aidance Skincare & Topical Solutions, LLC
Effective date
2025-08-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:09:15

Label at a glance#

ProductPM Recovery Pain Relief
Active ingredientMENTHOL, CAMPHOR (NATURAL)
Label structure9 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with strains, bruises and sprains.

Dosage and administration

Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: do not use, consult a physician. Wash hands after use with cool water.

Storage and handling

store at 20-25°C (68-77°F) store in a cool dry place away from direct sunlight

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor USP 10%

Menthol USP 15%

Purpose

OTC - PURPOSE SECTION

Camphor USP 10%..................External analgesic

Menthol USP 15%....................External analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with strains, bruises and sprains.

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product

  • avoid contact with eyes, nostrils and mouth
  • do not apply to wounds or damaged skin
  • do not bandage tightly

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily.
  • Children under 2 years of age: do not use, consult a physician.
  • Wash hands after use with cool water.

Other information

STORAGE AND HANDLING SECTION

  • store at 20-25°C (68-77°F)
  • store in a cool dry place away from direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beeswax, Honeysuckle Oil, Jojoba Oil, Lavender Oil, MCT Oil, Shea Butter

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-855-790-8169

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Charlotte's Web

PM Recovery

Muscle & Joint

Pain Relief Stick

Camphor 10% | Menthol 15%

Relaxing Essential Oils

NET WT. 1 OZ (30 G)

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2720403camphor 10 % / menthol 15 % Topical OilPSN1
2720403camphor 100 MG/ML / menthol 150 MG/ML Topical OilSCD1
2720403camphor 10 % / menthol 15 % Topical OilSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79845-770-30PM Recovery Pain Relief30 g in 1 CYLINDERSTICK301

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79845-77079845-770-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PM Recovery Pain ReliefCAMPHOR, MENTHOLCharlotte's Web, Inc.3aa08859-809d-de8c-e063-6394a90a8e252025-08-01WarningsExact identifier
ndc (package): 79845-770-30
ndc (product): 79845-770
ndc11 (package): 79845077030
spl id: 3aa08859-809e-de8c-e063-6394a90a8e25
spl set id: 3aa08859-809d-de8c-e063-6394a90a8e25

Reported adverse events (FAERS/openFDA)#

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