Home NDC 24286-1564 VAPOREX
Product NDC 24286-1564
11-digit product format 242861564
Labeler code 24286
Product ID 24286-1564_47d51ff5-fcae-89e2-e063-6294a90a03c2
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR (SYNTHETIC), EUCALYPTUS Oil, and MENTHOL
Dosage form OINTMENT
Route TOPICAL
Labeler DLC Laboratories, Inc.
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-03-12
Substance CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL, UNSPECIFIED FORM
Active strength 4.8; 1.2; 2.6 g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 VAPOREX
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 4.8 g/100g EUCALYPTUS OIL 1.2 g/100g MENTHOL, UNSPECIFIED FORM 2.6 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup 2R04ONI662 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 727137 Internal RxNorm lookup 1432507 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 24286-1564-2 VAPOREX 1 in 1 CARTON OINTMENT 1 4 24286-1564-2 VAPOREX 62.5 g in 1 JAR OINTMENT 62.5 4 24286-1564-3 VAPOREX 1 in 1 CARTON OINTMENT 1 4 24286-1564-3 VAPOREX 56.7 g in 1 JAR OINTMENT 56.7 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CAMPHOR (SYNTHETIC) ACTIVE INGREDIENT 5TJD82A1ET VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 EUCALYPTUS OIL ACTIVE INGREDIENT 2R04ONI662 VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 MENTHOL, UNSPECIFIED FORM ACTIVE INGREDIENT L7T10EIP3A VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 CAMPHOR (SYNTHETIC) ACTIVE MOIETY 5TJD82A1ET VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 EUCALYPTUS OIL ACTIVE MOIETY 2R04ONI662 VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 MENTHOL, UNSPECIFIED FORM ACTIVE MOIETY L7T10EIP3A VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 CEDAR LEAF OIL INACTIVE INGREDIENT BJ169U4NLG VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 NUTMEG OIL INACTIVE INGREDIENT Z1CLM48948 VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 PARAFFIN INACTIVE INGREDIENT I9O0E3H2ZE VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 PETROLATUM INACTIVE INGREDIENT 4T6H12BN9U VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 THYMOL INACTIVE INGREDIENT 3J50XA376E VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1 TURPENTINE OIL INACTIVE INGREDIENT C5H0QJ6V7F VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24286-1564 VAPOREX (CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL) OINTMENT [DLC LABORATORIES, INC.] 3 Current NDC, Legacy NDC, 4 package rows 20240514_971943b1-4199-4f75-9d2d-61242d346b5f.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 129 of 177 · 3,534 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Childrens Mucus and Cough Relief DEXTROMETHORPHAN HBR, GUAIFENESIN CARDINAL HEALTH 110, LLC. DBA LEADER 125eeb3d-0ee2-45bb-81c0-4ca699979886 2024-12-16 Warnings Exact identifier application number: M012 Dextromethorphan HBr 15 mg Liquid Gels DEXTROMETHORPHAN HBR RUGBY LABORATORIES cf3cc387-6642-43fd-999d-688fdaf65d4f 2024-12-14 Warnings Exact identifier application number: M012 Allergy Relief Dye-Free Softgel DIPHENHYDRAMINE HYDROCHLORIDE CVS PHARMACY, INC 60b1bb79-3ed1-438b-a27f-f7fbc108d114 2024-12-14 Warnings Exact identifier application number: M012 Rycontuss Cherry Flavor CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE Okendpharma, Inc. c91798fa-48ab-47a0-92da-4d44c2aafde0 2024-12-13 Warnings Exact identifier application number: M012 Mentholatum Lavender Vaporizing Rub CAMPHOR, EUCALYPTUS OIL, MENTHOL The Mentholatum Company 6f208c05-617d-492a-a016-e9d6be3c971f 2024-12-13 Warnings Exact identifier application number: M012 CVS Vapor Steam CAMPHOR (SYNTHETIC) CVS 49da2c40-afc5-5770-e054-00144ff88e88 2024-12-13 Warnings Exact identifier application number: M012 Kroger Daytime Cold and Flu Softgel ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE The Kroger Company e428dd83-c538-2a92-e053-2a95a90a0e16 2024-12-13 Warnings Exact identifier application number: M012 Kroger Nighttime Cold and Flu Softgel ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE The Kroger Company e46291c7-6f4d-46a2-e053-2a95a90a80a1 2024-12-13 Warnings Exact identifier application number: M012 Foster and Thrive Childrens Allergy Relief DIPHENHYDRAMINE HCL Strategic Sourcing Services LLC 7eaba464-5cdb-4bd4-b272-38fa108658d5 2024-12-13 Warnings Exact identifier application number: M012 SUDAFED OM Sinus Severe Original OXYMETAZOLINE HYDROCHLORIDE Kenvue Brands LLC 1d089074-3969-ce6e-e063-6294a90aa70c 2024-12-12 Warnings Exact identifier application number: M012 RIGHT REMEDIES Allergy Relief DIPHENHYDRAMINE HYDROCHLORIDE Strive Pharmaceuticals Inc b4fc014c-7c5f-46a4-bf13-57103b6fa018 2024-12-11 Warnings Exact identifier application number: M012 Diphenhydramine Hydrochloride 25mg DIPHENHYDRAMINE HYDROCHLORIDE 25MG Strive Pharmaceuticals Inc b440eb2e-4de9-2b65-e053-2995a90abda8 2024-12-11 Warnings Exact identifier application number: M012 Meijer Effervescent Cold Relief ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE Meijer Distribution Inc. 6933ca9d-a32d-d856-e053-2a91aa0a408e 2024-12-10 Warnings Exact identifier application number: M012 Effervescent Orange Cold Relief ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE Meijer Distribution Inc. 826b5c0d-7a75-bbf0-e053-2a91aa0aebd6 2024-12-10 Warnings Exact identifier application number: M012 DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC MENTHOL Ricola USA Inc. 09141018-37ba-4c93-9051-1ed129c448c1 2024-12-10 Warnings Exact identifier application number: M012 Original Herb Cough Drops MENTHOL Ricola USA Inc. 6ac9d95b-f6b9-4515-b126-697f8f839612 2024-12-10 Warnings Exact identifier application number: M012 THE ORIGINAL NATURAL HERB COUGH DROPS MENTHOL Ricola USA Inc. 989d1529-2875-47bf-81df-65494d62be7a 2024-12-10 Warnings Exact identifier application number: M012 DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC MENTHOL Ricola USA Inc. 82813342-2be2-4731-ae90-dbd5eed667a9 2024-12-10 Warnings Exact identifier application number: M012 MOUNTAIN HERB SUGAR FREE WITH STEVIA COUGH SUPPRESSANT ORAL ANESTHETIC MENTHOL Ricola USA Inc. b640a5d2-a7fe-486d-a65f-e7c993f950d6 2024-12-10 Warnings Exact identifier application number: M012 Sugar Free Mountain Herb Cough Suppressant Throat Drops MENTHOL Ricola USA Inc. c3f3c062-55e5-43c1-a016-ee47a7b388a5 2024-12-10 Warnings Exact identifier application number: M012
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 24286-1564-2 24286156402 1 in 1 CARTON Historical 24286-1564-3 24286156403 1 JAR in 1 CARTON (24286-1564-3) / 56.7 g in 1 JAR 1 jar 2013-03-12 0000-00-00 No No Current