Humphreys Bendito Alcoholado

Product NDC
0219-0203
11-digit product format
002190203
Labeler code
0219
Product ID
0219-0203_d9506518-f00e-4668-a65a-22b870bf0881
Type
HUMAN OTC DRUG
Nonproprietary name
menthol
Dosage form
LIQUID
Route
TOPICAL
Labeler
Humphreys Pharmacal, Incorporated
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
1972-01-11
Marketing end
0000-00-00
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
13 mg/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0219-0203-802020-12-29C16284748780-19855d018-eb25-cd31-e053-dbdaa90ab51aMonografía / Drug Facts
0219-0203-802019-11-27C16284748780-19855d018-eb25-cd31-e053-dbdaa90ab51aMonografía / Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0219-0203-80Humphreys Bendito Alcoholado237 mL in 1 BOTTLE, PLASTICLIQUID2375

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0219-0203HUMPHREYS BENDITO ALCOHOLADO (MENTHOL) LIQUID [HUMPHREYS PHARMACAL, INCORPORATED]5Legacy NDC, 1 package rows20241211_f3e86cb8-2da5-4f6c-8672-7c600f84a7a0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1370957menthol 1.25 % Topical SolutionPSNf3e86cb8-2da5-4f6c-8672-7c600f84a7a05
1370957menthol 12.5 MG/ML Topical SolutionSCDf3e86cb8-2da5-4f6c-8672-7c600f84a7a05
1370957menthol 1.25 % Topical SolutionSYf3e86cb8-2da5-4f6c-8672-7c600f84a7a05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0219-0203-8000219020380237 mL in 1 BOTTLE, PLASTIC (0219-0203-80) 237 ml1972-01-110000-00-00NoNoCurrent