- ACTIVE INGREDIENTS/PURPOSE
- USES
- WARNINGS
- PREGNANCY
- WARNINGS
- DIRECTIONS
- QUESTIONS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GAMMA -12
interleukin-12 human recombinant - interferon gamma-1b - solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17089-405 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength INTERFERON GAMMA-1B (UNII: 21K6M2I7AG) (INTERFERON GAMMA-1B - UNII:21K6M2I7AG) INTERFERON GAMMA-1B 4 [hp_C] in 30 mL INTERLEUKIN-12 HUMAN RECOMBINANT (UNII: 02FXP10O2U) (INTERLEUKIN-12 HUMAN RECOMBINANT - UNII:02FXP10O2U) INTERLEUKIN-12 HUMAN RECOMBINANT 4 [hp_C] in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) 9 mL in 30 mL Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17089-405-18 1 in 1 BOX 03/31/2011 1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/29/2010 Labeler - Guna spa (430538264) Establishment Name Address ID/FEI Business Operations Guna spa 338587646 manufacture(17089-405)