Label: POPULUS RADIX 6X liquid
- NDC Code(s): 53645-2340-6
- Packager: True Botanica, LLC
- 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 September 15, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- Use:
- Warnings:
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DO NOT USE
- Directions for Use:
- Other Ingredients:
- QUESTIONS
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
POPULUS RADIX 6X
populus radix 6x liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53645-2340 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS NIGRA WHOLE (UNII: D3JZE55MKS) (POPULUS NIGRA WHOLE - UNII:D3JZE55MKS) POPULUS NIGRA WHOLE 6 [hp_X] in 30 mL POPULUS DELTOIDES SUBSP. DELTOIDES WHOLE (UNII: GTJ6598VKZ) (POPULUS DELTOIDES SUBSP. DELTOIDES WHOLE - UNII:GTJ6598VKZ) POPULUS DELTOIDES SUBSP. DELTOIDES WHOLE 6 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53645-2340-6 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/14/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/14/2023 Labeler - True Botanica, LLC (182071519) Establishment Name Address ID/FEI Business Operations True Botanica, LLC 182071519 manufacture(53645-2340)