BLT 2 LIDOCAINE HCL CENTURA PHARMACEUTICALS INC FDA Approved USES For the temporary relief of pain and itching.
FunFoxMeds box
Route
TOPICAL
Applications
M017
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
ACTIVE INGREDIENT Lidocaine HCL 4%
Inactive Ingredients
INACTIVE INGREDIENTS Acrylates C10-30 Alkyl Acrylate Crosspolymer Aqua (Deionized Water) Beeswax Benzyl Alcohol Cetyl Alcohol Dehydroacetic Acid Glycerin Helianthus Anuus (Sunflower) Oil Polysorbate 20 Sodium Hydroxide Stearic Acid.
Strengths
4 %
Treats Conditions
Uses For The Temporary Relief Of Pain And Itching

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UPC
0647356934773
UNII
V13007Z41A
Packaging

PACKAGE LABELING BLT 2

Package Descriptions
  • PACKAGE LABELING BLT 2

Overview

USES For the temporary relief of pain and itching.

Indications & Usage

USES For the temporary relief of pain and itching.

Dosage & Administration

DIRECTIONS Adults and children two-years of age or older: Apply to affected area not more than three to four times daily. Children under two-years of age: consult a physician.

Warnings & Precautions
WARNINGS • For external use only. • Avoid contact with eyes or mucus membranes. • Do not apply to open or damaged skin. • If condition worsens or symptoms persist for more than seven days, discontinue use and consult physician. • If pregnant or breast feeding,contact physician prior to use. • Keep out of reach of children. If swallowed, contact Poison Control Center. • Do not use if allergic to any ingredient in ointment. • Do not use in large quantities, particularly over raw surfaces or blistered areas.
Purpose

PURPOSE Topical Anesthetic

Keep Out of Reach of Children

KEEP OUT OF REACH OF CHILDREN

Storage & Handling

OTHER INFORMATION Store below 77° F (25° C). Avoid direct sunlight.


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