Label: BELLIS PERENNIS KIT REFILL- bellis perennis pellet
- NDC Code(s): 71919-773-01
- Packager: Washington Homeopathic Products
- 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 June 10, 2022
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- ACTIVE INGREDIENTS
- USES
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS
- STOP USE AND ASK DOCTOR
- DIRECTIONS
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BELLIS PERENNIS KIT REFILL
bellis perennis pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71919-773 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BELLIS PERENNIS (UNII: 2HU33I03UY) (BELLIS PERENNIS - UNII:2HU33I03UY) BELLIS PERENNIS 200 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white (white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71919-773-01 350 in 1 VIAL, GLASS; Type 0: Not a Combination Product 06/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/10/2022 Labeler - Washington Homeopathic Products (084929389) Establishment Name Address ID/FEI Business Operations Washington Homeopathic Products 084929389 manufacture(71919-773)