Label: KIDS RELIEF- drosera, arnica montana, bryonia, ipecacuanha, cetraria islandica, coccus cacti, corallium rubrum, stannum metallicum liquid
- NDC Code(s): 71971-9121-4, 71971-9121-5, 71971-9121-9
- Packager: Homeolab International (Canada) 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.
Drug Label Information
Updated December 10, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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PURPOSE
Purpose
Drosera 1C............................dry cough
Arnica Montana 3C..................aches and pains, chest congestion
Bryonia 3C.............................painful cough
Ipecacuanha 3C......................night cough
Cetraria islandica 1C...............cough with expectoration
Coccus cacti 3C......................cough with expectoration
Corallium rubrum 3C...............painful cough
Stannum metallicum 3C...........coughs, chills and lessens mucus
The letters "HPUS" indicate that the components in this product are officially
monographed in the Homeopathic Pharmacopoeia of the United States.
- INDICATIONS & USAGE
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WARNINGS
Warnings
Stop use and ask a doctor if •pain or cough gets worse or lasts
more than 5 days ( children) or 7 days (adults) •fever gets worse
or lasts more than 3 days •redness or swelling is present •new
symptoms occur •cough comes back or occurs with rash or
headache that lasts. These could be signs of a serious condition.
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIDS RELIEF
drosera, arnica montana, bryonia, ipecacuanha, cetraria islandica, coccus cacti, corallium rubrum, stannum metallicum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71971-9121 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (DROSERA ROTUNDIFOLIA FLOWERING TOP - UNII:75O014T1HG) DROSERA ROTUNDIFOLIA FLOWERING TOP 1 [hp_C] in 100 mL ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 3 [hp_C] in 100 mL BRYONIA ALBA WHOLE (UNII: 56K0VVT47P) (BRYONIA ALBA WHOLE - UNII:56K0VVT47P) BRYONIA ALBA WHOLE 3 [hp_C] in 100 mL IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC 3 [hp_C] in 100 mL CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1) (CETRARIA ISLANDICA SUBSP. ISLANDICA - UNII:BJ7YPN79A1) CETRARIA ISLANDICA SUBSP. ISLANDICA 1 [hp_C] in 100 mL COCHINEAL (UNII: TZ8Z31B35M) (COCHINEAL - UNII:TZ8Z31B35M) COCHINEAL 3 [hp_C] in 100 mL CORALLIUM RUBRUM WHOLE (UNII: 22Z32PWR7R) (CORALLIUM RUBRUM WHOLE - UNII:22Z32PWR7R) CORALLIUM RUBRUM WHOLE 3 [hp_C] in 100 mL TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN 3 [hp_C] in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) CARAMEL (UNII: T9D99G2B1R) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71971-9121-9 1 in 1 CARTON 03/03/2018 1 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:71971-9121-5 1 in 1 CARTON 03/03/2018 2 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:71971-9121-4 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/03/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/03/2018 Labeler - Homeolab International (Canada) inc (203639455)
