FDA.reportPublic FDA data

Flexall Pain Relieving

Product NDC
41167-1602
11-digit product format
411671602
Labeler code
41167
Product ID
41167-1602_88efa8b4-48f8-4ba6-bcd4-9f66edf89dee
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Chattem, Inc.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
1997-01-01
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
0 g/g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1087519Flexall Maximum Strength 16 % Topical GelPSN79dd238d-87fe-4d89-bb3f-2677cae259931
253056menthol 16 % Topical GelPSN79dd238d-87fe-4d89-bb3f-2677cae259931
1087519menthol 0.16 MG/MG Topical Gel [Flexall]SBD79dd238d-87fe-4d89-bb3f-2677cae259931
253056menthol 0.16 MG/MG Topical GelSCD79dd238d-87fe-4d89-bb3f-2677cae259931
1087519Flexall 0.16 MG/MG Topical GelSY79dd238d-87fe-4d89-bb3f-2677cae259931
1087519Flexall Maximum Strength 16 % Topical GelSY79dd238d-87fe-4d89-bb3f-2677cae259931
253056menthol 16 % Topical GelSY79dd238d-87fe-4d89-bb3f-2677cae259931

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41167-1602-2411671602021 BOTTLE in 1 CARTON (41167-1602-2) > 85 g in 1 BOTTLE1 bottle1997-01-010000-00-00NoNoCurrent