Dry Eye Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Dry Eye Relief

Similasan Corporation

Similasan Dry Eye Relief Trial Size


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Belladonna* 6X

*containing 0.000002% alkaloids calculated as hyoscyamine.

Purpose

dryness, redness

Active Ingredient

Euphrasia 6X

Purpose

redness

Active Ingredient

Mercurius sublimatus 6X

Purpose

dryness

Dry Eye Relief Uses

According to homeopathic principles, the active ingredients in this medication temporarily relieve minor symptoms such as:

  • dry eye
  • redness of eyes and lids
  • reflex watering secondary to dry eye
  • sensation of grittiness
  • sensitivity to light

Warnings

  • For external use only.
  • Initial exacerbation of symptoms may occur.
  • Use only if single-use dropper is intact.
  • To avoid contamination, do not touch the tip of the dropper to any surface. Do not reuse. Once opened, discard.
  • Contact wearers: consult a physician prior to using.

Do not use:

if the solution changes color or becomes cloudy

Stop use and ask a doctor if:

  • symptoms worsen or persist for more than 72 hours.
  • changes in vision occur.
  • you experience eye pain.

If pregnant or breast feeding,

ask a health professional before use.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

For adults and children age 2 and over:

  • remove a single-use dropper
  • twist flat end with ball to remove
  • squeeze plastic dropper to release 2-3 drops into eye and discard applicator

Inactive Ingredients

Phosphate buffer, Purified water

Principal Display Panel

Homeopathic
NDC 59262-352-13
Similasan
Dry Eye Relief
Preservative Free
2 Single-Use sterile eye drops
0.45 ml/ 0.015 fl oz each
Dry Eye Relief


Principal Display Panel

SIMILASAN / USA
30011
Dry Eye Relief, eye drops
270 pieces(Stk)

Dry Eye Relief

Dry Eye Relief

Atropa Belladonna and Euphrasia Stricta and Mercuric Chloride SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59262-352
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ATROPA BELLADONNA ATROPA BELLADONNA 6 [hp_X]
EUPHRASIA STRICTA EUPHRASIA STRICTA 6 [hp_X]
MERCURIC CHLORIDE MERCURIC CATION 6 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
sodium phosphate, monobasic, dihydrate
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.45 in 1 VIAL, SINGLE-USE
2 NDC:59262-352-13 .45 in 1 VIAL, SINGLE-USE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-07-02


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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