Phoenix Balm

Product NDC
24438-001
11-digit product format
244380001
Labeler code
24438
Product ID
24438-001_fab49a9f-9c0f-4a00-81cf-c9bbd5ef0826
Type
HUMAN OTC DRUG
Nonproprietary name
Pain Relief Rub
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Amazonian Naturals, Inc.
Application
part348
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2011-12-01
Marketing end
0000-00-00
Substance
CAMPHOR (NATURAL); MENTHOL; METHYL SALICYLATE
Active strength
50 mg/g; mg/g; mg/g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
24438-001-022019-11-13C16284748780-197449f38-c65c-f6ea-e053-dbdaa90aa703Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24438-001-01Phoenix Balm19 g in 1 CONTAINEROINTMENT191
24438-001-02Phoenix Balm1 in 1 BOXOINTMENT11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24438-001PHOENIX BALM (PAIN RELIEF RUB) OINTMENT [AMAZONIAN NATURALS, INC.]1Legacy NDC, 2 package rows20111201_1ee482e2-155b-4f82-ab90-0457911806a8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1232398camphor 5 % / menthol 5 % / methyl salicylate 5 % Topical OintmentPSN1ee482e2-155b-4f82-ab90-0457911806a81
1232398camphor 0.05 MG/MG / menthol 0.05 MG/MG / methyl salicylate 0.05 MG/MG Topical OintmentSCD1ee482e2-155b-4f82-ab90-0457911806a81
1232398camphor 5 % / menthol 5 % / methyl salicylate 5 % Topical OintmentSY1ee482e2-155b-4f82-ab90-0457911806a81

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
24438-001-012443800010119 g in 1 CONTAINER19 gHistorical
24438-001-02244380001021 in 1 BOXHistorical