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Dry Eye Relief - 53799-351-12 - (Belladonna 6X, Euphrasia 6X, Mercurius sublimatus 6X)

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Drug Information of Dry Eye Relief

Product NDC: 53799-351
Proprietary Name: Dry Eye Relief
Non Proprietary Name: Belladonna 6X, Euphrasia 6X, Mercurius sublimatus 6X
Active Ingredient(s): 6; 6; 6    [hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL & nbsp;   Belladonna 6X, Euphrasia 6X, Mercurius sublimatus 6X
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Dry Eye Relief

Product NDC: 53799-351
Labeler Name: Similasan AG
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19850101

Package Information of Dry Eye Relief

Package NDC: 53799-351-12
Package Description: .45 mL in 1 VIAL, SINGLE-USE (53799-351-12)

NDC Information of Dry Eye Relief

NDC Code 53799-351-12
Proprietary Name Dry Eye Relief
Package Description .45 mL in 1 VIAL, SINGLE-USE (53799-351-12)
Product NDC 53799-351
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Belladonna 6X, Euphrasia 6X, Mercurius sublimatus 6X
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19850101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Similasan AG
Substance Name ATROPA BELLADONNA; EUPHRASIA STRICTA; MERCURIC CHLORIDE
Strength Number 6; 6; 6
Strength Unit [hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL
Pharmaceutical Classes

Complete Information of Dry Eye Relief


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