Label: T-42- butterfly pea solution
- NDC Code(s): 58264-0287-1
- Packager: DNA Labs, Inc.
- 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 May 16, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- INDICATIONS
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- WARNINGS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
T-42
butterfly pea solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0287 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLITORIA TERNATEA FLOWER (UNII: 1SYA8HK01B) (CLITORIA TERNATEA FLOWER - UNII:1SYA8HK01B) CLITORIA TERNATEA FLOWER 30 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58264-0287-1 29.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 05/16/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/16/2022 Labeler - DNA Labs, Inc. (031784339)