DR.LUKE SCIATICA AND NEUROPATHY PAIN RELIEF CREAM- sciatica and neuropathy pain relief cream 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.

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83176-003
DR.Luke SCIATICA & NEUROPATHY PAIN RELIEF CREAM

ACTIVE INGREDIENT

Mentho 3%

USES

For temporary pain relief the symptoms such as
Sciatica
Joints
Muscles strain & bruise
Neurophthy
Knees
Backache
Shoulder

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.


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 damaged skin(cuts, abrasions, eczema, sunburn)
lf You are pregnant or breast-feeding
lf You are allergic to this product.

Keep out of reach of children.

DO NOT USE

DO NOT USE
On damaged skin(cuts, abrasions, eczema, sunburn)
lf You are pregnant or breast-feeding
lf You are allergic to this product.

STOP USE AND SEE A DOCTOR IF

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

Centipede, Confligo, Bee Poison, Lacumlongagibb Erae Regulum,
Gecko, Nigerformicae, Chuanku, Caespes, Cnecos, Arnia, Msm, Lycopod,
Trglnta Septem, Independensvivis, Notopteryguy, Rhodiola, Strychnos, Borneol,
Chlorhexidine Acetate, Water

QUESTIONS?

drlukehealthcare.com
Info@drlukehealthcare.com

Pain Relief

83176-003-01

83176-003-01

DR.LUKE SCIATICA AND NEUROPATHY PAIN RELIEF CREAM 
sciatica and neuropathy pain relief cream cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83176-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL3 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ACONITUM CARMICHAELII ROOT (UNII: XJ28061U1S)  
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)  
STRYCHNOS MITIS WHOLE (UNII: 065A363355)  
NITRIC OXIDE SYNTHASE, ENDOTHELIAL (UNII: B3YWY5M7SW)  
GEKKO GECKO (UNII: 6HHE9M7R1C)  
SCOLOPENDRA SUBSPINIPES (UNII: T77DYH08RY)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83176-003-01100 mL in 1 BOTTLE; Type 0: Not a Combination Product01/22/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/22/2023
Labeler - Dr.luke Healthcare LLC (118868014)
Establishment
NameAddressID/FEIBusiness Operations
Dr.luke Healthcare LLC118868014label(83176-003) , manufacture(83176-003)

Revised: 1/2023
Document Id: f2d7294b-a299-b012-e053-2995a90a343b
Set id: f2d7294b-a298-b012-e053-2995a90a343b
Version: 1
Effective Time: 20230122
 
Dr.luke Healthcare LLC