Dr. Luke DMSO Cream

Manufacturer
DANOUS LAND FLOOW LLC
Effective date
2025-11-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:17:08

Label at a glance#

ProductDr. Luke DMSO Cream
Active ingredientARNICA MONTANA
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Arnica Montana Extract 1X HPUS 5%
Zingiber officinale 3XHPUS 3%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

Temporarily relieve discomfort caused by mild muscle and joint pain

WARNINGS SECTION

  • For external use only.

OTC - DO NOT USE SECTION

  • Do not apply to open wounds or broken skin.
  • You are allergic to Frankincense, Magnesium Chloride or other inactive ingredients in this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes, mucous membranes. If contact occurs, rinse with water
  • Perform a patch test before first use.DMSO can transport other substances through the skin. Use only on clean, intact skin.
  • A mild warming, cooling sensation, or garlic-like odor(DMSO characteristic) is normal.
  • Do not use it if pregnant or breastfeeding.
  • Consult your healthcare provider before use, especially if you are taking medications or have a medical condition.

OTC - STOP USE SECTION

  • excessive irritation or rash develops, discontinue use.
  • condition persists for more than 3 days or worsens
  • symptoms clear up and occur again within a few days.

OTC - ASK DOCTOR/PHARMACIST SECTION

consult a physician before use if you are pregnant or nursing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

INSTRUCTIONS FOR USE SECTION

Before use, Please wash your hands and clean the affected area with warm water.
Apply a small amount of the product to the affected area 2-3 times daily.
Gently massage until fully absorbed.

INACTIVE INGREDIENT SECTION

Water
Glycerol
Dimethyl Sulfoxide
Dimethyl Sulfone
Magnesium Chloride
Stearic Acid
Jojoba Oil
Arginine
Curcumin
Frankincense Extract
Hydrogenated Lecithin
Vitamin E
Xanthan Gum

OTHER SAFETY INFORMATION

  • Do not use if glued carton end flaps are open or if the tube seal is broken.
  • Store at 68°-77°F (20°-25C).
  • Keep container tightly closed

DOSAGE & ADMINISTRATION SECTION

Apply a small amount of the product to the affected area 2-3 times daily.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87147-006-01Dr. Luke DMSO Cream114 g in 1 JARCREAM1141

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87147-00687147-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
43f8512e-7bfb-ed91-e063-6394a90a92e743f84d44-18eb-7f88-e063-6394a90ab3d52025-11-19WarningsExact identifier
spl id: 43f8512e-7bfb-ed91-e063-6394a90a92e7
spl set id: 43f84d44-18eb-7f88-e063-6394a90ab3d5

Reported adverse events (FAERS/openFDA)#

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