AVALIN-RX- lidocaine and menthol patch 
RXCHANGE CO

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.

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For external use only

Do not use

  • in large quantities, particulary ove raw surfaces or blistered areas
  • other than directed by a doctor
  • on open wounds or damaged skin
  • with a bandage to cover the surface
  • for longer than 5 consecrutive days

Ask a doctor before use if used for children under 12.

When using this product avoid contact with the eyes.

Stop use and ask a doctor

  • conditions worsens
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

If pregnant or breast-feeding, ask a health professional before use.

Keep ou rof reach of children. If swallowed, get medical help or contact Poinson Control Center right away.

Acrylic acid, aluminum hydroxide, carmellose sodium, 2-ethylhexyl acrylate, glycerin, isopropyl myristate, methyl acrylate, nonoxynol-30, polyacrylate, polyacrylic acid, polysorvate 80, sorbitan sesquioleate, starch, talc, tartaric acid, titanium dioxide, water

  • Adults and children 12 years of age and older: Apply to the affected area not more than 3 to 4 times daily.
  • Children under 12 years of age: Consult a doctor.
  • Clean and dry affected area.
  • Remove patch from backing and apply to affected area.
  • Use one patch at a time.
  • Leave patch on affected area for up to 8-hours at a time.

Store in dry area between 59-79 F (15-26 C).

Rx-Only

NDC 33358-0925-15

Avalin-Rx

Lidocaine 4% and Menthol 1%

External Analgesic Patch

For the temporary relief of pain associated with minor cuts, scrapes, and minor skin irritations.

15 patches

PRINCIPLE DISPLAY PANEL

Manufactured for: RxChange Co.

Burbank, CA 91504

Made in China.

Patent pending

Active Ingredients

Lidocaine 4%

Menthol 1%

Purpose: External Analgesics

AVALIN-RX 
lidocaine, menthol patch
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:33358-925
Route of AdministrationTOPICAL, TRANSDERMALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
Colorwhite (WHITE COATED RECTANGULAR PATCH) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:33358-925-15100 g in 1 CARTON; Type 0: Not a Combination Product
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/201506/16/2015
Labeler - RXCHANGE CO (781126805)
Establishment
NameAddressID/FEIBusiness Operations
WUHAN FULAI PHARMACEUTICAL TECHNOLOGY CO LTD420782368manufacture(33358-925)

Revised: 6/2015
 
RXCHANGE CO