Label: SYMBIO FORTI DROPS- penicillium roqueforti liquid
- NDC Code(s): 69710-185-11
- Packager: Symbiopathic
- 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 December 11, 2024
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- ACTIVE INGREDIENTS:
- WARNINGS:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- KEEP OUT OF REACH OF CHILDREN:
- INDICATIONS:
- QUESTIONS:
- PURPOSE:
- If pregnant or breast feeding...
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- OTHER INFORMATION:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
SYMBIO FORTI DROPS
penicillium roqueforti liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69710-185 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L) PENICILLIUM ROQUEFORTI 4 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69710-185-11 1 in 1 CARTON 10/08/2023 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 10/08/2023 Labeler - Symbiopathic (202697595) Establishment Name Address ID/FEI Business Operations Deserving Health International Corp 202617023 manufacture(69710-185)