Label: THYMUS VULGARIS (N)- thyme tincture
- NDC Code(s): 13838-1447-1
- Packager: Phytodyne 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.
Updated October 23, 2018
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- INACTIVE INGREDIENT
PRINCIPAL DISPLAY PANEL - 20 ml Bottle Label
Thymus vulgaris Ø (N)
Use: For temporay relief of asthma and spastic cough
Directions : Adults and children above 12 years: 2-5
drops 1-3 times daily in pure water before meals. Consult
a physician for use in children under 12 years of age.
0.67 fl.oz. (20ml)
INGREDIENTS AND APPEARANCE
THYMUS VULGARIS (N)
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:13838-1447 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength THYME (UNII: CW657OBU4N) (THYME - UNII:CW657OBU4N) THYME 1 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Product Characteristics Color BROWN Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13838-1447-1 20 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/01/2005 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 10/01/2005 Labeler - Phytodyne Inc. (164980927)