Cannaflex

Manufacturer
ALLURE LABS INC.
Effective date
2019-10-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:01:19

Label at a glance#

ProductCannaflex
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: Temporarily relieves minor pain associated with arthritis, backache, muscle strains, muscle sprains, bruises, cramps. 

WARNINGS SECTION

Warning: For external use only.

OTC - ASK DOCTOR SECTION

Allergy alert if prone to allergic reaction from aspirin or salicylates, consult a Doctor before use.

OTC - WHEN USING SECTION

When using this product: Use only as directed. Read and follow all directions and warnings on this label. Do not bandage tightly or use with a heated pad. Avoid contact with eyes or mucous membranes. Do not apply to wounds or damaged, broken or irritated skin. Do not use at the same time with other topical analgesics.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens. Symptoms persist for more than 7 days or clear up and occur again within a few days. Redness is persistent. Irritation develops.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Coconut Alkanes, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Methyl Sulfonyl Methane, Stearic Acid, Glycerin, Aesculus Hippocastannum (Horse Chestnut) Seed Extract, Rosa Moschata Seed Oil, Menthoxypropanediol, Sorbitan Olivate, Cannabidiol (From full spectrum hemp extract), Medium Chain Triglyceride, Cetearyl Olivate, Phenoxyethanol, Menthyl Lactate, Tocopherol, Mentha Piperita (Pepperment) Oil, Cetyl Palmitate, Sorbitan Palmitate, Coco-Caprylate/Caprate, Caprylyl Glycol, Menthol, Xanthan Gum, Ethylhexylglycerin, Hexylene Glycol, Vanillyl Butyl Ether.

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years: Apply generously to affected area. Massage into painful area until thoroughly asborbed into skin. Repeat as necessary, But no more than 4 times daily.

OTC - QUESTIONS SECTION

Questions or Comments? 

Call our customer service department at: 1-800-898-5153 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Manufactured for:

CBD Therapeutics, LLC

Salt Lake City, UT 84116

ImageCannaflexImageCannaflex

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62742-4177-22023-01-30C16284748780-1f386c64a-1915-0266-e053-dadaa90a7c1aDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62742-4177-1Cannaflex45 mL in 1 TUBECREAM451
62742-4177-2Cannaflex1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62742-4177CANNAFLEX (TROLAMINE SALICYLATE) CREAM [ALLURE LABS INC.]1Legacy NDC, 2 package rows20191026_59b4a7d3-5805-4d0f-8080-9efc5813dc49.zip

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62742-417762742-4177-1, 62742-4177-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 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
78c39b0d-6458-4115-857a-a4d9ae0dd14c59b4a7d3-5805-4d0f-8080-9efc5813dc492019-10-16WarningsExact identifier
spl id: 78c39b0d-6458-4115-857a-a4d9ae0dd14c
spl set id: 59b4a7d3-5805-4d0f-8080-9efc5813dc49

Reported adverse events (FAERS/openFDA)#

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