NEURACIN TOPICAL GEL- neuracin topical analgesic gel gel

Neuracin Topical Gel by

Drug Labeling and Warnings

Neuracin Topical Gel by is a Otc medication manufactured, distributed, or labeled by SOLA Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Camphor 4%

Menthol 10%

Methyl Salicylate 30%

Purpose

Topical Analgesic

Uses

Temporarily relieves minor pain associated with:

• Arthritis
• Simple Backache
• Muscle Strains
• Bruises
• Muscle Sprains

Warnings

For External use only

When using this product

• avoid contact with eyes and mucous membranes
• do no apply to wounds or damaged skin
• do not bandage tightly or use with a heating pad
• use only as directed

Stop use and ask a doctor if condition worsens; symptoms last more than 7 days or clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help right away. If pregnant Or Breast-Feeding, Ask A Health Professional Before Use

Directions

• Apply on affected area, not more than 3 to 4 times daily
• Children under 12 years of age; consult a doctor

Other Information

• Store at 20-25ºC (68-77ºF) Store away from heat

Inactive Ingredients

Benzyl alcohol, Carbomer, Pemulen, Polysorbate 80, Purified Water, Triethanolamine

PRINCIPAL DISPLAY PANEL

Questions or comments? Call 1-866-747-7365

Neuracin Topical Analgesic Gel

NDC: 70512-104-60

Qty 2oz (56.7G)

INGREDIENTS AND APPEARANCE

NEURACIN TOPICAL GEL 
neuracin topical analgesic gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70512-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	300 mg  in 1 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	40 mg  in 1 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	100 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
CARBOMER 940 (UNII: 4Q93RCW27E)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70512-104-60	1 in 1 CARTON	05/24/2021
1		56.7 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/24/2021

Labeler - SOLA Pharmaceuticals (080121345)