Home NDC 72197-046 Pharmacys Prescription Vapor Rub
Product NDC 72197-046
11-digit product format 721970046
Labeler code 72197
Product ID 72197-046_31aa4b96-eb44-f42a-e063-6294a90ac37a
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form GEL
Route TOPICAL
Labeler American Consumer Products Corp
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-02-09
Substance MENTHOL, UNSPECIFIED FORM; EUCALYPTUS OIL; CAMPHOR (SYNTHETIC)
Active strength 1.25; 1.2; 4.7 g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
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 Pharmacys Prescription Vapor Rub
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 1.25 g/100g EUCALYPTUS OIL 1.2 g/100g CAMPHOR (SYNTHETIC) 4.7 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 2R04ONI662 Internal UNII lookup 5TJD82A1ET Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2045202 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72197-046-04 Pharmacys Prescription Vapor Rub 110 g in 1 BOTTLE, PLASTIC GEL 110 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72197-046 PHARMACYS PRESCRIPTION VAPOR RUB (MENTHOL) GEL [AMERICAN CONSUMER PRODUCTS CORP] 1 Current NDC, 1 package rows 20250403_31aa54d8-df8d-f1ae-e063-6294a90a9622.zip
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 97 of 177 · 3,534 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 72197-046-04 72197004604 110 g in 1 BOTTLE, PLASTIC (72197-046-04) 110 g 2025-03-31 No No Current