Label: REMEDI HEALTH SOLUTIONS DIMINISH GLUTEN REACTIVITY- anatherum muricatum, avena sativa, arsenicum album, berberis vulgaris, dioscorea villosa, okoubaka aubrevillei spray
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Contains inactivated NDC Code(s)
NDC Code(s): 59985-323-32 - Packager: Chc Montana
- 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 January 6, 2021
If you are a consumer or patient please visit this version.
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- DRUG FACTS
- HPUS Active Ingredients
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Purpose
ANATHERUM MURICATUM 6c, 30c.............................. Grain allergy
AVENA SATIVA 6c, 30c.............................................. Calming, Soothing
ARSENICUM ALBUM 6c, 30c....................................... Restless Bloated Stomach & Bowel
BERBERIS VULGARIS 6c, 30c...................................... Painful Gas
DIOSCOREA VILLOSA 6c, 30c.................................... Cramping, pain in gut
OKOUBAKA AUBREVILLEI 6c, 30c................................ Wheat sensitivity - USES
- WARNINGS
- DIRECTIONS
- Inactive Ingredients:
- Questions/Comments? Side Effects?
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SPL UNCLASSIFIED SECTION
Authentic Time-Tested Health Products
soothing, comfort for gluten distress
SPEED RELIEF
Homeopathic remedies have been effective and safe for over 200 years.
SUGAR FREE
DAIRY FREE
SOY FREE
GLUTEN FREE
NON-GMOCustomers love our products!
SATISFACTION GUARANTEED
No known drug interactions
HIGH POTENCY
FASTER ACTING100% Natural • 100% Drug Free
Fast Acting • Zero Side Effects
Safe for All AgesHOMEOPATHELLENSTURBO®
PO Box 6
Stevensville, MT 59870
Toll Free (855) 777-5875
RemediHealthSolutions.com
Since 1993Manufactured by: PURE SOURCE LLC
9750 NW17th St., Miami, FL 33172NDC# 5998532332
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INGREDIENTS AND APPEARANCE
REMEDI HEALTH SOLUTIONS DIMINISH GLUTEN REACTIVITY
anatherum muricatum, avena sativa, arsenicum album, berberis vulgaris, dioscorea villosa, okoubaka aubrevillei sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59985-323 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHRYSOPOGON ZIZANIOIDES ROOT (UNII: 37TB8LUP9Z) (CHRYSOPOGON ZIZANIOIDES ROOT - UNII:37TB8LUP9Z) CHRYSOPOGON ZIZANIOIDES ROOT 30 [hp_C] in 30 mL AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (AVENA SATIVA FLOWERING TOP - UNII:MA9CQJ3F7F) AVENA SATIVA FLOWERING TOP 30 [hp_C] in 30 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 30 [hp_C] in 30 mL BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 6 [hp_C] in 30 mL DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8) (DIOSCOREA VILLOSA ROOT - UNII:IWY3IWX2G8) DIOSCOREA VILLOSA TUBER 6 [hp_C] in 30 mL OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z) (OKOUBAKA AUBREVILLEI BARK - UNII:MK2074187Z) OKOUBAKA AUBREVILLEI BARK 6 [hp_C] in 30 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59985-323-32 1 in 1 BOX 01/01/2019 1 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/2019 Labeler - Chc Montana (101745243)