KIDS RELIEF TEETHING ORAL LIQUID- chamomilla, arnica montana, borax, hypericum perforatum liquid liquid

Kids Relief by

Drug Labeling and Warnings

Kids Relief by is a Homeopathic medication manufactured, distributed, or labeled by Homeolab International (Canada) inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients HPUS:

Chamomilla (German chamomile) 5C

Arnica montana (Leopard's bane) 5C

Borax (Sodium borate) 5C

Hypericum perforatum ( St John's wort) 5C

PURPOSE

Purpose

Gum pain, restlessness, irritability and agitation

Toothache and fever

Gum inflammation and diarrhea

Dental nerve pain

The letters 'HPUS' indicate that the components in this product are officially monographed in the Homoeopathic Pharmacopoeia of the United States.

INDICATIONS & USAGE

Uses

This homeopathic medicine is made from a combination of ingredients traditionally used to help relieve indispositions caused by teething*:

gum inflammation

gum pain

fever

diarrhea

restlessness and irritability

WARNINGS

Warnings

Do not use if imprinted shrink seal neckband is broken or missing.

Stop use and ask a doctor in cases of high fever or if symptoms worsen or persist for more than 3 days.

KEEP OUT OF REACH OF CHILDREN

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 2 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.

STORAGE AND HANDLING

Other Information

Store at room temperature.   

INACTIVE INGREDIENT

Inactive Ingredients

Purified water, sorbitol, sodium benzoate, potassium sorbate, citric acid, orange oil.

PRINCIPAL DISPLAY PANEL

LABEL

PRINCIPAL DISPLAY PANEL

CARTON

INGREDIENTS AND APPEARANCE

KIDS RELIEF  TEETHING ORAL LIQUID
chamomilla, arnica montana, borax, hypericum perforatum liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71971-9060
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ)	MATRICARIA RECUTITA	5 [hp_C]  in 25 mL
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	5 [hp_C]  in 25 mL
SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22)	SODIUM BORATE	5 [hp_C]  in 25 mL
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	5 [hp_C]  in 25 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Characteristics
Color		Score
Shape		Size
Flavor	ORANGE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71971-9060-8	1 in 1 CARTON	03/03/2017
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		03/03/2017

Labeler - Homeolab International (Canada) inc (203639455)

Registrant - Homeolab International (Canada) inc (203639455)