Label: HERPETIC NOSODE 4012- herpetic nosode liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 63083-4012-2 - Packager: Professional Complementary Health Formulas
- 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 August 15, 2019
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- QUESTIONS
- INDICATIONS
- PURPOSE
-
WARNINGS
Severe or persistent symptoms may be a sign of a serious condition. Consult a doctor promptly if symptoms persist or are accompanied by a fever. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- LABEL
-
INGREDIENTS AND APPEARANCE
HERPETIC NOSODE 4012
herpetic nosode liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-4012 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL) (HUMAN HERPESVIRUS 1 - UNII:22G38P19RL) HUMAN HERPESVIRUS 1 30 [hp_X] in 59 mL HUMAN HERPESVIRUS 6 (UNII: 4IX4VP35CR) (HUMAN HERPESVIRUS 6 - UNII:4IX4VP35CR) HUMAN HERPESVIRUS 6 30 [hp_X] in 59 mL HUMAN HERPESVIRUS 7 (UNII: 1L6FS9X8O1) (HUMAN HERPESVIRUS 7 - UNII:1L6FS9X8O1) HUMAN HERPESVIRUS 7 30 [hp_X] in 59 mL HUMAN HERPESVIRUS 8 (UNII: 16I9IX46F2) (HUMAN HERPESVIRUS 8 - UNII:16I9IX46F2) HUMAN HERPESVIRUS 8 30 [hp_X] in 59 mL RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN (UNII: COB9FF6I46) (RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN - UNII:COB9FF6I46) RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN 30 [hp_X] in 59 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:63083-4012-2 59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/15/1985 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/15/1984 Labeler - Professional Complementary Health Formulas (167339027) Registrant - Natural Pharmaceutical Manufacturing LLC (015624923) Establishment Name Address ID/FEI Business Operations Natural Pharmaceutical Manufacturing LLC 015624923 manufacture(63083-4012)