Home NDC 84126-383 Vicks VapoFreeze
Product NDC 84126-383
11-digit product format 841260383
Labeler code 84126
Product ID 84126-383_5d192f10-056a-e376-e063-6394a90a54e1
Type HUMAN OTC DRUG
Nonproprietary name Camphor, Menthol
Dosage form LIQUID
Route TOPICAL
Labeler The Procter & Gamble Manufacturing Company
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-05
Substance CAMPHOR (SYNTHETIC); LEVOMENTHOL
Active strength 3.6; 16 g/100g; g/100g
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 Vicks VapoFreeze
Brand name suffix PAIN RELIEF
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 3.6 g/100g LEVOMENTHOL 16 g/100g
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84126-383-03 Vicks VapoFreezePAIN RELIEF 70.9 g in 1 BOTTLE, WITH APPLICATOR LIQUID 70.9 1
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 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84126-383-03 84126038303 70.9 g in 1 BOTTLE, WITH APPLICATOR (84126-383-03) 70.9 g 2026-05-05 No No Current