Home NDC 72197-007 Pharmacys Prescription Vapor Rub
Product NDC 72197-007
11-digit product format 721970007
Labeler code 72197
Product ID 72197-007_2c69c634-e137-1428-e063-6294a90aa8f1
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 2018-09-28
Substance EUCALYPTUS OIL; CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM
Active strength 1; 4.7; 1 g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 72197-007-04 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 72197-007-04 0efc9e666f02…f202fb6c5f17…
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 EUCALYPTUS OIL 1 g/100g CAMPHOR (SYNTHETIC) 4.7 g/100g MENTHOL, UNSPECIFIED FORM 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2R04ONI662 Internal UNII lookup 5TJD82A1ET Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1042788 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 72197-007-04 Pharmacys Prescription Vapor Rub 110 g in 1 BOTTLE, PLASTIC GEL 110 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72197-007 PHARMACYS PRESCRIPTION VAPOR RUB (MENTHOL) GEL [AMERICAN CONSUMER PRODUCTS CORP] 4 Current NDC, Legacy NDC, 1 package rows 20250125_6ef328ff-f5c3-515d-e053-2a91aa0a32d3.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 74 of 180 · 3,583 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72197-007-04 72197000704 110 g in 1 BOTTLE, PLASTIC (72197-007-04) 110 g 2018-09-28 0000-00-00 No No Current