Label: ANAGALLIS ARVENSIS globule
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Contains inactivated NDC Code(s)
NDC Code(s): 53645-2050-3 - Packager: True Botanica, LLC
- 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 January 30, 2021
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- Official Label (Printer Friendly)
- 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
ANAGALLIS ARVENSIS
anagallis arvensis globuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53645-2050 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAGALLIS ARVENSIS (UNII: 46883LR90E) (ANAGALLIS ARVENSIS - UNII:46883LR90E) ANAGALLIS ARVENSIS 30 [hp_X] in 23 g Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53645-2050-3 23 g in 1 BOTTLE; Type 0: Not a Combination Product 02/03/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/03/2014 Labeler - True Botanica, LLC (182071519) Establishment Name Address ID/FEI Business Operations True Botanica, LLC 182071519 manufacture(53645-2050)