![H PYLORI REMEDY (HELICOBACTER PYLORI) LIQUID [DESERET BIOLOGICALS, INC.]](https://medic.hrt.org//dailymed/images/3812219f-0171-4098-a32c-60f9615a8fd9/DSRT535 H. Pylori Remedy 6-27-16.jpg)
- ACTIVE INGREDIENT:
- HOMEOPATHIC INDICATIONS:
For the temporary relief of symptoms related to H. Pylori infection including upper abdominal pain or discomfort, loss of appetite, belching, nausea, vomiting and fatigue.**
**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Close - WARNINGS:
Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.
If pregnant or breast-feeding, ask a health professional before use.
Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.
Close - KEEP OUT OF REACH OF CHILDREN:
Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.
Close - DIRECTIONS:
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
Close - HOMEOPATHIC INDICATIONS:
For the temporary relief of symptoms related to H. Pylori infection including upper abdominal pain or discomfort, loss of appetite, belching, nausea, vomiting and fatigue.**
**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Close - INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
- INGREDIENTS AND APPEARANCE
H PYLORI REMEDY
helicobacter pylori liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0802 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HELICOBACTER PYLORI (UNII: U09W5JOL3Z) (HELICOBACTER PYLORI - UNII:U09W5JOL3Z) HELICOBACTER PYLORI 15 [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:43742-0802-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 07/06/2016 08/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/06/2016 08/04/2021 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) CloseEstablishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-0802) , api manufacture(43742-0802) , label(43742-0802) , pack(43742-0802)
