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Natralia Cramp Relief - 43251-3213-4 - (Methyl Salicylate)

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Drug Information of Natralia Cramp Relief

Product NDC: 43251-3213
Proprietary Name: Natralia Cramp Relief
Non Proprietary Name: Methyl Salicylate
Active Ingredient(s): 105    mg/g & nbsp;   Methyl Salicylate
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Natralia Cramp Relief

Product NDC: 43251-3213
Labeler Name: Laderma Trading Pty Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20090301

Package Information of Natralia Cramp Relief

Package NDC: 43251-3213-4
Package Description: 3 g in 1 PACKET (43251-3213-4)

NDC Information of Natralia Cramp Relief

NDC Code 43251-3213-4
Proprietary Name Natralia Cramp Relief
Package Description 3 g in 1 PACKET (43251-3213-4)
Product NDC 43251-3213
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Methyl Salicylate
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20090301
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Laderma Trading Pty Ltd
Substance Name METHYL SALICYLATE
Strength Number 105
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Natralia Cramp Relief


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