Home NDC 51316-118 CVS Pain Relief Lavender Scent
Product NDC 51316-118
11-digit product format 513160118
Labeler code 51316
Product ID 51316-118_484b0833-9f89-f155-e063-6294a90a1869
Type HUMAN OTC DRUG
Nonproprietary name Menthol 4%
Dosage form GEL
Route TOPICAL
Labeler CVS
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-01
Substance MENTHOL, (+)-
Active strength 4 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base CVS Pain Relief Lavender Scent
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, (+)- 4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C6B1OE8P3W Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 415974 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 109 of 151 · 3,020 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 51316-118-02 51316011802 74 mL in 1 BOTTLE, PLASTIC (51316-118-02) 74 ml 2026-06-01 No No Current 51316-118-03 51316011803 89 mL in 1 TUBE (51316-118-03) 89 ml 2026-06-01 No No Current