Label: OHM-PAN- carbo vegetabilis, ceanothus americanus, gallium aparine, leptandra virginica, mandragora officinarum, momordica balsamina, quassia amara spray
- NDC Code(s): 66096-759-02
- Packager: OHM PHARMA INC.
- Category: HUMAN PRESCRIPTION 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 28, 2021
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
OHM-PAN
carbo vegetabilis, ceanothus americanus, gallium aparine, leptandra virginica, mandragora officinarum, momordica balsamina, quassia amara sprayProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66096-759 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 12 [hp_X] in 30 mL CEANOTHUS AMERICANUS LEAF (UNII: 25B1Y14T8N) (CEANOTHUS AMERICANUS LEAF - UNII:25B1Y14T8N) CEANOTHUS AMERICANUS LEAF 10 [hp_X] in 30 mL GALIUM APARINE (UNII: Z4B6561488) (GALIUM APARINE - UNII:Z4B6561488) GALIUM APARINE 5 [hp_X] in 30 mL VERONICASTRUM VIRGINICUM ROOT (UNII: M2O62YTN42) (CULVER'S ROOT - UNII:M2O62YTN42) VERONICASTRUM VIRGINICUM ROOT 5 [hp_X] in 30 mL MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB) MANDRAGORA OFFICINARUM ROOT 10 [hp_X] in 30 mL MOMORDICA BALSAMINA IMMATURE FRUIT (UNII: WUW1665V10) (MOMORDICA BALSAMINA IMMATURE FRUIT - UNII:WUW1665V10) MOMORDICA BALSAMINA IMMATURE FRUIT 8 [hp_X] in 30 mL QUASSIA AMARA WOOD (UNII: S5249Q85HW) (QUASSIA AMARA WOOD - UNII:S5249Q85HW) QUASSIA AMARA WOOD 5 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66096-759-02 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/19/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/19/2018 Labeler - OHM PHARMA INC. (030572478)
