CBD Pain Relief Cream

Manufacturer
Allure Labs
Effective date
2024-12-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:41:03

Label at a glance#

ProductCBD Pain Relief Cream
Active ingredientTROLAMINE SALICYLATE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Trolamine Salicylate 10%

OTC - PURPOSE SECTION

Purpose:

Topical Analgesic

INDICATIONS & USAGE SECTION

Uses: For temporary relief of minor aches and pains of the muscles and joints (such as arthritis, backache, sprains and bruises).

WARNINGS SECTION

Warnings:

  • For external use only
  • Keep out of reach of children

OTC - WHEN USING SECTION

When using this product

  • use only as directed
  • do not bandage tightly or use with a heating pad
  • avoid contact eith eyes or mucus membranes
  • do not apply to wounds or damaged skin

OTC - STOP USE SECTION

Stop use and ask a doctor if:

  • Condition worsens
  • symptoms persists for more tham 7 days or clear up and occurs again within few days.
  • Redness is present
  • irritaiotn develops

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breat feeding

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.

DOSAGE & ADMINISTRATION SECTION

Directions:

Adults and children over 12 years of age:
• Apply generously to affected area
• massage into painful area until thoroughly absorbed into skin
• repeat as necessary, but no more than 4 times daily

OTC - ASK DOCTOR SECTION

Children 12 years or younger:
• Ask a doctor

OTHER SAFETY INFORMATION

Other Information
• Store at room temperature

ALLERGY ALERT - If prone to allergic reaction from aspirin orsalicylates, consult a doctor before use.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Aqua), Coconut Alkanes*, Sorbitan Olivate*, Cetearyl Olivate*, Glycerin*, Dimethyl Sulfone, Glyceryl Stearate*,Cannabidiol (From Hemp Extract), Stearic Acid*, Cetyl Palmitate*, Rosa Moschata Seed Oil*, Cetearyl Alcohol, Ceteareth-20, Sorbitan Palmitate*, Tocopherol, Vanillyl Butyl Ether, Coco-Caprylate/Caprate*, Caprylhydroxamic acid*, Glyceryl Caprylate*, Xanthan Gum*

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Manufactured for

DermaQuest®, Inc.

Hayward CA-94544

Made In USA

dermaquestinc.com

IMGCBDPRCIMGCBDPRC

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62742-4198-1CBD Pain Relief Cream57 g in 1 TUBECREAM572

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62742-4198CBD PAIN RELIEF CREAM (TROLAMINE SALICYLATE) CREAM [ALLURE LABS]2Current NDC, Legacy NDC, 1 package rows20241208_b6b3102a-4154-2da2-e053-2995a90ae99f.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62742-419862742-4198-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
CBD Pain Relief CreamTROLAMINE SALICYLATEAllure Labsb6b3102a-4154-2da2-e053-2995a90ae99f2024-12-05WarningsExact identifier
ndc (package): 62742-4198-1
ndc (product): 62742-4198
ndc11 (package): 62742419801
spl id: 288ef7b4-3328-1b0f-e063-6394a90ad09d
spl set id: b6b3102a-4154-2da2-e053-2995a90ae99f

Reported adverse events (FAERS/openFDA)#

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