Label: PARIS QUADRIFOLIA pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 15631-0330-0, 15631-0330-1, 15631-0330-2, 15631-0330-3, view more15631-0330-4, 15631-0330-5 - Packager: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
- 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 March 24, 2020
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- ACTIVE INGREDIENT
- USES
- INDICATIONS
- DOSAGE
- WARNINGS
- INACTIVE INGREDIENTS
- STORAGE
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QUESTIONS OR COMMENTS
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INGREDIENTS AND APPEARANCE
PARIS QUADRIFOLIA
paris quadrifolia pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:15631-0330 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PARIS QUADRIFOLIA (UNII: PME3ETQ5WQ) (PARIS QUADRIFOLIA - UNII:PME3ETQ5WQ) PARIS QUADRIFOLIA 3 [hp_X] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:15631-0330-0 100 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 2 NDC:15631-0330-1 200 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 3 NDC:15631-0330-2 400 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 4 NDC:15631-0330-3 750 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 5 NDC:15631-0330-4 2500 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 6 NDC:15631-0330-5 12500 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/12/2015 Labeler - Rxhomeo Private Limited d.b.a. Rxhomeo, Inc (650833994) Establishment Name Address ID/FEI Business Operations Rxhomeo Private Limited d.b.a. Rxhomeo, Inc 650833994 manufacture(15631-0330) , label(15631-0330)