Label: IMMUNITEA HERBAL RELIEF TEA- cinnamon, ginger, licorice, holy basil leaf, litsea glutinosa bark granule, for solution
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Contains inactivated NDC Code(s)
NDC Code(s): 75360-1145-1 - Packager: Hemani International
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated October 4, 2022
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SPL UNCLASSIFIED SECTION
Immunitea Herbal Relief Tea is manufactured using only the following ingredients in the preparation of the product (percentage in final product formulation base off of 2g unit measure of each herbal tea bag content contains the following:
- Cinnamon 420mg 21%
- Ginger 420mg 21%
- Licorice 400mg 20%
- Holy Basil Leaf 360mg 17%
- Litsea Glutinosa Bark 340mg 18%
- Artemisa Absinthium 60mg 3%
The firm does not add other active or inactive ingredients.
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
IMMUNITEA HERBAL RELIEF TEA
cinnamon, ginger, licorice, holy basil leaf, litsea glutinosa bark granule, for solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75360-1145 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CINNAMON (UNII: 5S29HWU6QB) (CINNAMON - UNII:5S29HWU6QB) CINNAMON 420 mg in 2 g LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883) LICORICE 400 mg in 2 g LITSEA GLUTINOSA BARK (UNII: 41SI4SQJ7R) (LITSEA GLUTINOSA BARK - UNII:41SI4SQJ7R) LITSEA GLUTINOSA BARK 340 mg in 2 g HOLY BASIL LEAF (UNII: SCJ765569P) (HOLY BASIL LEAF - UNII:SCJ765569P) HOLY BASIL LEAF 360 mg in 2 g GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 420 mg in 2 g Inactive Ingredients Ingredient Name Strength ARTEMISIA ABSINTHIUM WHOLE (UNII: 51PW3BIW1K) 60 mg in 2 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75360-1145-1 28 g in 1 BOX, UNIT-DOSE; Type 0: Not a Combination Product 07/22/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/22/2020 Labeler - Hemani International (645581294) Registrant - Hemani International (645581294) Establishment Name Address ID/FEI Business Operations Hemani International 645581294 manufacture(75360-1145)