- SPL UNCLASSIFIED SECTION
- INDICATIONS
- INGREDIENTS
- Rx CAUTION
- SUGGESTED DOSAGE
- STORAGE AND HANDLING
- Warnings
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 2 FL. OZ. Bottle Label
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INGREDIENTS AND APPEARANCE
G-41
ulmus glabra whole solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0404 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ULMUS GLABRA WHOLE (UNII: I2AHJ0JD5V) (ULMUS GLABRA WHOLE - UNII:I2AHJ0JD5V) ULMUS GLABRA WHOLE 1 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength Alcohol (UNII: 3K9958V90M) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58264-0404-2 59.14 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/01/1990 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 01/01/1990 Labeler - DNA Labs, Inc. (031784339)