Label: SYMBIO QUENT DROPS- penicillium frequentans liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69711-175-11 - Packager: Symbiopathic
- 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 May 15, 2023
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- ACTIVE INGREDIENTS:
- WARNINGS:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- KEEP OUT OF REACH OF CHILDREN:
- INDICATIONS:
- QUESTIONS:
- PURPOSE:
- If pregnant or breast feeding...
- ASK DOCTOR:
- OTHER INFORMATION:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
SYMBIO QUENT DROPS
penicillium frequentans liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69711-175 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PENICILLIUM GLABRUM (UNII: 2IN23YUE0I) (PENICILLIUM GLABRUM - UNII:2IN23YUE0I) PENICILLIUM GLABRUM 4 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69711-175-11 1 in 1 CARTON 08/25/2016 1 10 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/25/2016 Labeler - Symbiopathic (079767886) Establishment Name Address ID/FEI Business Operations Biological Health Group Corporation 079767886 manufacture(69711-175)