Label: BEYOND NICOTINE- kali sulph, nicotinum , plantago and tabacum spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 58214-789-01 - Packager: JMSP USA LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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 June 12, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingrdietns
- Purpose of ingredients:
- Keep out of reach of children
- Warnings:
- Indications and Usage:
- Inactive Ingredients:
- Directions
- Product Label
-
INGREDIENTS AND APPEARANCE
BEYOND NICOTINE
kali sulph, nicotinum , plantago and tabacum sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58214-789 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM SULFATE 6 [hp_X] in 30 mL NICOTINE (UNII: 6M3C89ZY6R) (NICOTINE - UNII:6M3C89ZY6R) NICOTINE 9 in 30 mL PLANTAGO MAJOR (UNII: W2469WNO6U) (PLANTAGO MAJOR - UNII:W2469WNO6U) PLANTAGO MAJOR 9 in 30 mL TOBACCO LEAF (UNII: 6YR2608RSU) (TOBACCO LEAF - UNII:6YR2608RSU) TOBACCO LEAF 9 in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58214-789-01 30 mL in 1 PACKAGE; Type 0: Not a Combination Product 06/11/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2017 Labeler - JMSP USA LLC (078770235) Registrant - JMSP USA LLC (078770235) Establishment Name Address ID/FEI Business Operations W Last CC 567284153 manufacture(58214-789)