RX300 Topical Pain Cream

Product NDC
79884-001
11-digit product format
798840001
Labeler code
79884
Product ID
79884-001_f117d2cd-ada3-c746-e053-2995a90a0ebb
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, LIDOCAINE
Dosage form
CREAM
Route
TOPICAL
Labeler
BENERX LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-08-01
Marketing end
0000-00-00
Substance
LIDOCAINE; MENTHOL
Active strength
4 g/100g; g/100g
Pharmacologic classes
Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79884-001-02798840001021 TUBE in 1 BOX (79884-001-02) > 88 g in 1 TUBE (79884-001-01) 1 tube2020-08-010000-00-00NoNoCurrent