Label: REMEDI HEALTH SOLUTIONS SUNBURN RELIEF- calendula officinalis, capsicum annuum, cantharis vesicatoria spray
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Contains inactivated NDC Code(s)
NDC Code(s): 59985-315-32 - 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
- Purpose
- USES
- WARNINGS
- DIRECTIONS
- Inactive Ingredients:
- Questions/Comments? Side Effects?
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SPL UNCLASSIFIED SECTION
Authentic Time-Tested Health Products
Diminish peeling, stinging & blistering
Homeopathic remedies have been effective and safe for over 200 years.
SUGAR FREE
DAIRY FREE
SOY FREE
GLUTEN FREE
NON-GMOCustomers love this product!
SATISFACTION GUARANTEED
VACATION SAVER!
Relief for urgent pain & blistering.
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
Since 1993
Toll Free (855) 777-5875
RemediHealthSolutions.comManufactured by: PURE SOURCE LLC
9750 NW17th St., Miami, FL 33172NDC# 5998531532
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INGREDIENTS AND APPEARANCE
REMEDI HEALTH SOLUTIONS SUNBURN RELIEF
calendula officinalis, capsicum annuum, cantharis vesicatoria sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59985-315 Route of Administration ORAL, TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP 30 [hp_C] in 30 mL CAPSICUM ANNUUM WHOLE (UNII: 7FKZ3QQQ1F) (CAPSICUM ANNUUM WHOLE - UNII:7FKZ3QQQ1F) CAPSICUM ANNUUM WHOLE 30 [hp_C] in 30 mL LYTTA VESICATORIA (UNII: 3Q034RO3BT) (LYTTA VESICATORIA - UNII:3Q034RO3BT) LYTTA VESICATORIA 30 [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:59985-315-32 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)