CVS Lidocaine Pain Relief Dry

Product NDC
66902-257
Requested package NDC
66902-257-04
11-digit product format
669020257
Labeler code
66902
Product ID
66902-257_bfc32759-707f-41b1-afbe-81484ed48d29
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, UNSPECIFIED FORM, LIDOCAINE
Dosage form
SPRAY
Route
TOPICAL
Labeler
Natural Essentials, Inc.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-01-21
Marketing end
0000-00-00
Substance
MENTHOL, UNSPECIFIED FORM; LIDOCAINE
Active strength
10 mg/g; mg/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Reported adverse events (FAERS/openFDA)#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66902-257CVS LIDOCAINE PAIN RELIEF DRY (MENTHOL, UNSPECIFIED FORM, LIDOCAINE) SPRAY [NATURAL ESSENTIALS, INC.]3Legacy NDC20241004_c20a4954-df80-4dce-9582-8b49e2a497bb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66902-257-0466902025704113 g in 1 CAN (66902-257-04) 113 g2021-01-210000-00-00NoNoCurrent