Veltrix

VELTRIX- lidocaine and menthol cream
Home Aide Diagnostics, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

PURPOSE: Topical analgesic


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

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
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

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

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VELTRIX
veltrix pain relieiving cream cream
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69379-004
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE (LIDOCAINE) LIDOCAINE 4 g in 100 g
MENTHOL (MENTHOL) MENTHOL 1 g in 100 g
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69379-004-03 120 g in 1 BOTTLE None
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 Operations
Zhejiang Bangli Medical Products Cl. Ltd. 421295875 manufacture (69379-004)

Revised: 07/2015 Home Aide Diagnostics, Inc.

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