Cleanize - 44929-001-02 - (sodium chloride)

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Drug Information of Cleanize

Product NDC: 44929-001
Proprietary Name: Cleanize
Non Proprietary Name: sodium chloride
Active Ingredient(s): 900    mg/100mL & nbsp;   sodium chloride
Administration Route(s): NASAL; OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cleanize

Product NDC: 44929-001
Labeler Name: Laboratoires Gifrer Barbezat
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20081125

Package Information of Cleanize

Package NDC: 44929-001-02
Package Description: 20 AMPULE in 1 CARTON (44929-001-02) > 5 mL in 1 AMPULE (44929-001-01)

NDC Information of Cleanize

NDC Code 44929-001-02
Proprietary Name Cleanize
Package Description 20 AMPULE in 1 CARTON (44929-001-02) > 5 mL in 1 AMPULE (44929-001-01)
Product NDC 44929-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name sodium chloride
Dosage Form Name SOLUTION
Route Name NASAL; OPHTHALMIC
Start Marketing Date 20081125
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Laboratoires Gifrer Barbezat
Substance Name SODIUM CHLORIDE
Strength Number 900
Strength Unit mg/100mL
Pharmaceutical Classes

Complete Information of Cleanize


General Information