Label: ANACARDIUM liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 53645-1491-3 - 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 December 19, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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
- Anarcardium Orientale 30X
-
INGREDIENTS AND APPEARANCE
ANACARDIUM
anacardium liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53645-1491 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (ANACARDIUM OCCIDENTALE FRUIT - UNII:4A10JR4E7E) ANACARDIUM OCCIDENTALE FRUIT 30 [hp_X] in 55 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 30 [hp_X] in 55 mL Product Characteristics Color Score Shape FREEFORM Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53645-1491-3 55 mL 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(53645-1491)