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ManzanillaSophia - 57619-400-01 - (Chamomile (Matricaria Chamomilla L.))

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Drug Information of ManzanillaSophia

Product NDC: 57619-400
Proprietary Name: ManzanillaSophia
Non Proprietary Name: Chamomile (Matricaria Chamomilla L.)
Active Ingredient(s): 3    [hp_X]/mL & nbsp;   Chamomile (Matricaria Chamomilla L.)
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of ManzanillaSophia

Product NDC: 57619-400
Labeler Name: LABORATORIOS SOPHIA, S.A. DE C.V.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100412

Package Information of ManzanillaSophia

Package NDC: 57619-400-01
Package Description: 1 BOTTLE, PLASTIC in 1 PACKAGE (57619-400-01) > 15 mL in 1 BOTTLE, PLASTIC

NDC Information of ManzanillaSophia

NDC Code 57619-400-01
Proprietary Name ManzanillaSophia
Package Description 1 BOTTLE, PLASTIC in 1 PACKAGE (57619-400-01) > 15 mL in 1 BOTTLE, PLASTIC
Product NDC 57619-400
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Chamomile (Matricaria Chamomilla L.)
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20100412
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name LABORATORIOS SOPHIA, S.A. DE C.V.
Substance Name MATRICARIA RECUTITA
Strength Number 3
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of ManzanillaSophia


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