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Salonpas DEEP Relieving - 55328-900-02 - (Camphor, Menthol, Methyl salicylate)

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Drug Information of Salonpas DEEP Relieving

Product NDC: 55328-900
Proprietary Name: Salonpas DEEP Relieving
Non Proprietary Name: Camphor, Menthol, Methyl salicylate
Active Ingredient(s): 3.1; 10; 15    g/100g; g/100g; g/100g & nbsp;   Camphor, Menthol, Methyl salicylate
Administration Route(s): PERCUTANEOUS; TOPICAL; TRANSDERMAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Salonpas DEEP Relieving

Product NDC: 55328-900
Labeler Name: Hisamitsu America, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130601

Package Information of Salonpas DEEP Relieving

Package NDC: 55328-900-02
Package Description: 1 TUBE in 1 BOX (55328-900-02) > 78 g in 1 TUBE

NDC Information of Salonpas DEEP Relieving

NDC Code 55328-900-02
Proprietary Name Salonpas DEEP Relieving
Package Description 1 TUBE in 1 BOX (55328-900-02) > 78 g in 1 TUBE
Product NDC 55328-900
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Camphor, Menthol, Methyl salicylate
Dosage Form Name GEL
Route Name PERCUTANEOUS; TOPICAL; TRANSDERMAL
Start Marketing Date 20130601
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Hisamitsu America, Inc.
Substance Name CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Strength Number 3.1; 10; 15
Strength Unit g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of Salonpas DEEP Relieving


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