VELTRIX- veltrix pain relieiving cream cream

Veltrix by

Drug Labeling and Warnings

Veltrix by is a Prescription medication manufactured, distributed, or labeled by Home Aide Diagnostics, Inc., Zhejiang Bangli Medical Products Cl. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INFORMATION FOR PATIENTS

PURPOSE: Topical analgesic

ACTIVE INGREDIENTS
Lidocain 4% --------------------------------------------------------------------------------------------------------- Topical analgesic
Menthol 1% --------------------------------------------------------------------------------------------------------- Topical analgesic

INDICATIONS & USAGE

INDICATIONS
For the temporary relief of pain of muscles and joints associated with:

• Arthritis
• Simple Backache
• Strains
• Sprains
• Bruises

DIRECTIONS
Adults and children over 12 years
Apply generously to affected area
Massage into painful area until thoroughly absorbed into skin, repeat as necessary, not more than 3-4 times daily
Store at 20°-25°C (68°-77 °F). Avoid direct sunlight.

WARNINGS

WARNINGS
FOR EXTERNAL USE ONLY.

• When using this product use only as directed
• Do not bandage tightly
• Do not use with a heating pad
• Agoid contact with the eyes or mucous membranes
• Do not apply to wounds or damaged or irritated skin

WARNINGS AND PRECAUTIONS

STOP USE AND ASK A DOCTOR IF

• Condition worsens
• Symptoms persist for more than 7 days or clear up and occur again within a few days
• Redness is present
• Irritation develops

OTHER SAFETY INFORMATION

• Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
• If pregnant of breast-feeding, ask a healthcare professional before use

INACTIVE INGREDIENT

INACTIVE INGREDIENTS
aliphatic alcohol; stearic acid; vaseline; peregal; Carmellose; odium; water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VELTRIX 
veltrix pain relieiving cream cream

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 69379-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69379-004-03	120 g in 1 BOTTLE; Type 0: Not a Combination Product	07/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/01/2015

Labeler - Home Aide Diagnostics, Inc. (783518983)

Registrant - Zhejiang Bangli Medical Products Cl. Ltd. (421295875)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Bangli Medical Products Cl. Ltd.		421295875	manufacture(69379-004)