Label: ADRENAL liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53645-1040-0 - 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 February 8, 2013
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- 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
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
ADRENAL
adrenal liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53645-1040 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (BOS TAURUS ADRENAL GLAND - UNII:M2776SWB29) BOS TAURUS ADRENAL GLAND 6 [hp_X] in 50 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53645-1040-0 50 mL in 1 BOTTLE, WITH APPLICATOR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/08/2013 Labeler - True Botanica, LLC (182071519) Establishment Name Address ID/FEI Business Operations True Botanica, LLC 182071519 manufacture(53645-1040)