NUVALU ICE THERAPY MENTHOL PAIN RELIEVING

Product NDC
76176-222
Requested package NDC
76176-222-24
11-digit product format
761760222
Labeler code
76176
Product ID
76176-222_7b8ee331-4847-f0bf-e053-2991aa0a13ea
Type
HUMAN OTC DRUG
Nonproprietary name
menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Ningbo Liyuan Daily Chemical Products Co., Ltd.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-11-01
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
1 g/100g
NDC exclude flag
No
Listing certified through
2020-12-31
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
76176-222-2476176022224227 g in 1 JAR (76176-222-24) 227 g2018-11-010000-00-00NoNoCurrent