NEUROMED 7 TOPICAL PAIN RELIEF- lidocaine hydrochloride cream 
Sambria Pharmaceuticals, LLC

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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 irritations.

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

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NEUROMED 7 TOPICAL PAIN RELIEF 
lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54723-175
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
WATER (UNII: 059QF0KO0R)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)  
EMU OIL (UNII: 344821WD61)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54723-175-221 in 1 CARTON04/13/2016
163 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/15/2013
Labeler - Sambria Pharmaceuticals, LLC (078676259)
Establishment
NameAddressID/FEIBusiness Operations
A.I.G. Technologies, Inc.086365223manufacture(54723-175) , label(54723-175) , pack(54723-175)

Revised: 12/2023
Document Id: 0b78e757-351a-9b38-e063-6394a90a145a
Set id: f199f56b-d971-4cf8-834d-babb5c2ff81a
Version: 12
Effective Time: 20231201
 
Sambria Pharmaceuticals, LLC