OTC Medication Information: OHEAL ARTHRITIS PAIN RELIEF Cream

OHEAL ARTHRITIS PAIN RELIEF CREAM- menthol cream
Dr.luke Healthcare LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ACTIVE INGREDIENT

Mentho 3%

USES

For arthritis, aching joints, neuropathy, sore muscles, tenosynovitis, frozen shoulder

WARNINGS

Avoid contacting with eyes, flush with water immediately if it gets into eyes.
Children should use it under the supervision of adults.
Keep out of reach of children.

WARNINGS
For external use only.
Avoid contacting with eyes, flush with water immediately if it gets into eyes.
Children should use it under the supervision of adults.
Keep out of reach of children.

DO NOT USE
On broken skin
On eyes area

Keep out of reach of children.

DO NOT USE

DO NOT USE

On broken skin
On eyes area

STOP USE AND SEE A DOCTOR IF

STOP USING AND SEE A DOCTOR IF.
If you are allergic to this product.
If you are pregnant or breast-feeding
You become pregnant, or are planning to become pregnant, while using this product

DIRECTION

DIRECTIONS
Apply to the effected areas 2-3 times daily, massage it and wait for it dry.

OTHER INGREDIENTS

Water, Aloe Vera, Centipede, Confligo, Lacumlongagibb Erae Regulum,
Sweet orange oil, Gecko, Nigerformicae, Chuanku,
Caespes, Emu Oil, Cnecos, Arnica, MSM, Lycopod, Trglnta Septem,
Independensvivis, Notopteryguy, Rhodiola, Strychnos, Borneol, Chlorhexidine Acetate.

QUESTIONS?

www.ohealpro.com Info@ohealpro.com

Pain Relief

83176-002-01

83176-002-01
(click image for full-size original)
OHEAL ARTHRITIS PAIN RELIEF CREAM arthritis pain relief cream cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:83176-002
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (MENTHOL) MENTHOL 3 mg in 100 mL
Inactive Ingredients
Ingredient Name Strength
RHODIOLA CRENULATA WHOLE
EMU OIL
ALOE VERA LEAF
BORNEOL
ACONITUM CARMICHAELII ROOT
SCOLOPENDRA SUBSPINIPES
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:83176-002-01 100 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 01/22/2023
Labeler — Dr.luke Healthcare LLC (118868014)
Establishment
Name Address ID/FEI Operations
Dr.luke Healthcare LLC 118868014 label (83176-002), manufacture (83176-002)

Revised: 01/2023 Dr.luke Healthcare LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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