BANIFLU  - gelsemium sempervirens root, influenza a virus a/new caledonia/20/99 (h1n1) antigen (propiolactone inactivated), influenza a virus a/panama/2007/99 (h3n2) antigen (propiolactone inactivated), influenza b virus b/hong kong/330/2001 antigen (propiolactone inactivated) and strychnos nux-vomica seed tablet 
Native Remedies, LLC

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

----------

BaniFlu

Supports protection during cold and flu season

Active Ingredients: Each dose contains equal parts of: Gelsemium 30C HPUS, Influenzinum 30C HPUS, Nux vom 30C HPUS.

Uses: Homeopathic remedy for immune support during cold and flu season.

Warnings: If symptoms persist or worsen, consult a healthcare professional.

If pregnant or breastfeeding, ask a health professional before use.

Keep this and all medication out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions: Adults: Dissolve 2 tablets in a clean mouth 3 times daily for 7 days prior to the winter season or before traveling. Repeat every 3 months or if exposed to infection. Babies and small children: Take 1/4 of adult serving, crush tablet, and sprinkle onto tongue.

Special instructions: Avoid strong mint-flavored candy.

Inactive Ingredients: Acacia gum, lactose, magnesium stearate, corn starch, sucrose.

The letters HPUS indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.com

Distributed by
Native Remedies, LLC
6531 Park of Commerce Blvd.
Suite 160
Boca Raton, FL 33487
Phone: +1.877.289.1235
International: +1.561.999.8857

Contains no artificial flavors or artificial colors. No gluten added.

Tamper resistant seal for your protection. Use only if safety seal is intact.

Bottle label

BANIFLU  
gelsemium, influenzinum, nux vom tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:68703-035
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]
INFLUENZA A VIRUS A/NEW CALEDONIA/20/99 (H1N1) ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 3NPZ4Z3B94) (INFLUENZA A VIRUS A/NEW CALEDONIA/20/99 (H1N1) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) - UNII:I2F6HCP28X) INFLUENZA A VIRUS A/NEW CALEDONIA/20/99 (H1N1) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) 30 [hp_C]
INFLUENZA A VIRUS A/PANAMA/2007/99 (H3N2) ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 2UES30W1DF) (INFLUENZA A VIRUS A/PANAMA/2007/99 (H3N2) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) - UNII:A08BMU572N) INFLUENZA A VIRUS A/PANAMA/2007/99 (H3N2) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) 30 [hp_C]
INFLUENZA B VIRUS B/HONG KONG/330/2001 ANTIGEN (PROPIOLACTONE INACTIVATED) (UNII: 23CET7LDKD) (INFLUENZA B VIRUS B/HONG KONG/330/2001 HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) - UNII:502XN5489H) INFLUENZA B VIRUS B/HONG KONG/330/2001 HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) 30 [hp_C]
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 30 [hp_C]
Inactive Ingredients
Ingredient Name Strength
ACACIA (UNII: 5C5403N26O)  
LACTOSE (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
STARCH, CORN (UNII: O8232NY3SJ)  
SUCROSE (UNII: C151H8M554)  
Product Characteristics
Color white (White lactose tablets) Score no score
Shape ROUND (Round lactose tablets) Size 6mm
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68703-035-80 180 in 1 BOTTLE, GLASS
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 01/02/2013
Labeler - Native Remedies, LLC (192014186)
Establishment
Name Address ID/FEI Business Operations
King Bio 617901350 api manufacture(68703-035) , manufacture(68703-035)

Revised: 1/2013
Document Id: e54cf84c-cbe9-4b12-b584-2066829440b7
Set id: 8c35f401-dce0-434f-a755-a5aedde16c76
Version: 2
Effective Time: 20130102
 
Native Remedies, LLC