CHAMOMILE HOMEOPATHIC EYE DROPS solution/ drops

Chamomile Homeopathic Eye Drops by

Drug Labeling and Warnings

Chamomile Homeopathic Eye Drops by is a Homeopathic medication manufactured, distributed, or labeled by HomeoCare Laboratories Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Inactive ingredients

Purified water
Sodium chloride
Sodium phosphate di-basic
Potassium phosphate
Benzalkonium chloride

Purpose

Dryness

Inflammation

DOSAGE & ADMINISTRATION

Uses To refresh and replenish moisture to eyes.
Directions 2 drops in each eye as needed.
To avoid contamination, do not touch tip of dropper to any surface.
Replace cap immediately after use.
Store at room temperature.
Use within 30 days of opening.

Warnings

For ophtalmic use only. Keep out of the reach of chlidren. Do not use is solution changes color or becomes cloudy. Discard 30 days after opening. Stop use and ask a doctor if you experience eye pain, changes in vision, redness or irritation of the eye. If conditions persist or worsen for more than 72 hours, discontinue use and consult your physician.

Do not use is cap safety band is torn or missing.

Active Ingredients

Chamomilla 3X HPUS

INDICATIONS & USAGE

Uses To refresh and replenish moisture to eyes.
Directions 2 drops in each eye as needed.
To avoid contamination, do not touch tip of dropper to any surface.
Replace cap immediately after use.
Store at room temperature.
Use within 30 days of opening.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

Label

SterileEyeDropsSri.jpg

Chamomile Homeopathic Eye Drops

INGREDIENTS AND APPEARANCE

CHAMOMILE HOMEOPATHIC EYE DROPS 
chamomile homeopathic eye drops solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61727-346(NDC:70696-346)
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MATRICARIA CHAMOMILLA WHOLE (UNII: 2Z4LRR776S) (MATRICARIA CHAMOMILLA WHOLE - UNII:2Z4LRR776S)	MATRICARIA CHAMOMILLA WHOLE	3 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61727-346-15	15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/23/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/23/2016

Labeler - HomeoCare Laboratories Inc. (088248828)

Registrant - HomeoCare Laboratories Inc. (088248828)

Establishment
Name	Address	ID/FEI	Business Operations
HomeoCare Laboratories Inc.		088248828	relabel(61727-346)