Label: KIDS RELIEF- pulsatilla, allium cepa, arsenicum album, nux vomica, euphrasia offinalis, sabadilla, aralia racemosa, cuprum metallicum liquid
- NDC Code(s): 71971-9066-8
- 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 July 25, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
PURPOSE
Purpose
Sinus symptoms, sneezing, nasal congestion, runny nose, itchy eyes, nose and throat, watery eyes headache, throat irritation.
The letters 'HPUS' indicate that the components in this product are officially monographed in the Homoeopathic Pharmacopoeia of the United States.
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated - INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions
Children under 6 months of age: Consult a licensed healthcare practitioner before using this product.
Children 6 months to 9 years old: 0.5 ml orally every 8 hours or 3 times a day.
Children 2 to 9 years old: 0.75 ml orally every 8 hours or 3 times a day.
Reduce intake with improvements.
In acute phase only:
Children 2 to 9 years old; Give 1 dropper (0.75ml) at the onset of symptoms. Repeat two more times at intervals of 15 minutes.
Repeat this procedure up to 6 times per day if symptoms reoccur, or as directed by a healthcare practitioner.
Not to be taken with meals - STORAGE AND HANDLING
- INACTIVE INGREDIENT
- Kids Relief Sinus Oral Liquid
-
INGREDIENTS AND APPEARANCE
KIDS RELIEF
pulsatilla, allium cepa, arsenicum album, nux vomica, euphrasia offinalis, sabadilla, aralia racemosa, cuprum metallicum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71971-9066 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANEMONE PULSATILLA (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) ANEMONE PULSATILLA 8 [hp_X] in 25 mL ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 6 [hp_X] in 25 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 8 [hp_X] in 25 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 6 [hp_X] in 25 mL EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 6 [hp_X] in 25 mL SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED 6 [hp_X] in 25 mL ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (ARALIA RACEMOSA ROOT - UNII:T90W4582DU) ARALIA RACEMOSA ROOT 6 [hp_X] in 25 mL COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 8 [hp_X] in 25 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CITRIC ACID ACETATE (UNII: DSO12WL7AU) RASPBERRY (UNII: 4N14V5R27W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71971-9066-8 1 in 1 CARTON 07/26/2019 1 25 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/26/2019 Labeler - Homeolab International (Canada) inc (203639455)
