Label: ASPERGILLUS- aspergillus niger var. niger suppository
- 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.
Updated January 29, 2016
If you are a consumer or patient please visit this version.
If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before using this product.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 10 Suppository Blister Pack Box
INGREDIENTS AND APPEARANCE
aspergillus niger var. niger suppository
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54256-029 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Aspergillus Niger Var. Niger (UNII: 9IOA40ANG6) (Aspergillus Niger Var. Niger - UNII:9IOA40ANG6) Aspergillus Niger Var. Niger 3 [hp_X] Inactive Ingredients Ingredient Name Strength Fat, Hard (UNII: 8334LX7S21) Sodium chloride (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54256-029-04 1 in 1 BOX 1 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 10/10/2015 Labeler - BioResource Inc. (017532917) Establishment Name Address ID/FEI Business Operations RubiePharm Arzneimittel GmbH 313767774 MANUFACTURE(54256-029)