Label: GAMMA -12- interleukin-12 human recombinant - interferon gamma-1b - solution/ drops
- NDC Code(s): 17089-405-18
- Packager: Guna spa
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated November 15, 2022
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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 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)