Skip to Content

NeuroMed 7 Topical Pain Relief

Dosage form: cream
Ingredients: LIDOCAINE HYDROCHLORIDE 4g in 100g
Labeler: Sambria Pharmaceuticals, LLC
NDC Code: 54723-175

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.

NeuroMed 7 Topical Pain Relief Cream

Active Ingredients

Lidocaine HCL 4.0% w/w

Purpose

External Anesthetic

Uses

For temporary relief of pain and itching due to minor skin irritation.

Warnings

- For external use only.

- Avoid contact with eyes.

- ​Do not use ​in large quantities, particularly over raw surfaces or blistered areas.

- ​Stop use and ask a doctor ​if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.  Discontinue use.

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

Directions

For adults and children two-years or older: Apply to affected area not more than 3 or 4 times daily.  Children under 2 years of age: consult a physician.

​Inactive Ingredients

Aqua (Deionized Water), Arnica Montana Floweri Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmenthane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine.

​Other Information

Protect this product from excessive heat and direct sun.

​Questions or Comments?

FDA Registered: NDC No 54723-175-22

info@sambriapharma.com

NEUROMED 7 TOPICAL PAIN RELIEF 
lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54723-175
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER 
ARNICA MONTANA FLOWER 
C13-14 ISOPARAFFIN 
SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) 
EMU OIL 
DIETHYLENE GLYCOL MONOETHYL ETHER 
ETHYLHEXYLGLYCERIN 
GLUCOSAMINE SULFATE 
ISOPROPYL PALMITATE 
MELALEUCA ALTERNIFOLIA LEAF 
DIMETHYL SULFONE 
PHENOXYETHANOL 
PROPYLENE GLYCOL 
STEARIC ACID 
TROLAMINE 
Packaging
#Item CodePackage Description
1NDC:54723-175-221 TUBE in 1 CARTON
163 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34808/15/2013
Labeler - Sambria Pharmaceuticals, LLC (078676259)
Establishment
NameAddressID/FEIOperations
A.I.G. Technologies, Inc.171837367manufacture(54723-175)

Revised: 06/2016
 
Sambria Pharmaceuticals, LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide