Natralia Cramp Relief

Product NDC
43251-3213
11-digit product format
432513213
Labeler code
43251
Product ID
43251-3213_b76aa734-54d8-4a3f-aefd-963d68b1051c
Type
HUMAN OTC DRUG
Nonproprietary name
Methyl Salicylate
Dosage form
GEL
Route
TOPICAL
Labeler
Laderma Trading Pty Ltd
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2009-03-01
Marketing end
0000-00-00
Substance
METHYL SALICYLATE
Active strength
105 mg/g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43251-3213-3Natralia Cramp Relief56 g in 1 TUBEGEL561
43251-3213-3Natralia Cramp Relief1 in 1 CARTONGEL11
43251-3213-4Natralia Cramp Relief3 g in 1 PACKETGEL31

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43251-3213NATRALIA CRAMP RELIEF (METHYL SALICYLATE) GEL [LADERMA TRADING PTY LTD]1Legacy NDC, 3 package rows20110329_d6c85b92-08bc-45de-9cec-43e49c707670.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1094875methyl salicylate 10.5 % Topical GelPSNd6c85b92-08bc-45de-9cec-43e49c7076701
1094875methyl salicylate 0.105 MG/MG Topical GelSCDd6c85b92-08bc-45de-9cec-43e49c7076701
1094875methyl salicylate 10.5 % Topical GelSYd6c85b92-08bc-45de-9cec-43e49c7076701

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
43251-3213-34325132130356 g in 1 TUBE56 gHistorical
43251-3213-4432513213043 g in 1 PACKET3 gHistorical