FDA.reportPublic FDA data

Mentholatum Childrens Nighttime Vaporizing Rub

Product NDC
10742-1112
11-digit product format
107421112
Labeler code
10742
Product ID
10742-1112_a717aa03-2f1d-4c69-bf00-d9888a9f1c95
Type
HUMAN OTC DRUG
Nonproprietary name
camphor, eucalyptus oil, menthol
Dosage form
OINTMENT
Route
TOPICAL
Labeler
The Mentholatum Company
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2018-08-01
Marketing end
0000-00-00
Substance
CAMPHOR (NATURAL); EUCALYPTUS OIL; MENTHOL, UNSPECIFIED FORM
Active strength
53 mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct10742-1112DDiscontinued by firm2026-10-05
excluded packagepackage10742-111210742-1112-1DDiscontinued by firm2026-10-05
excluded packagepackage10742-111210742-1112-2DDiscontinued by firm2026-10-05
excluded packagepackage10742-111210742-1112-3DDiscontinued by firm2026-10-05

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.

Dataset, Scope, Package NDC table
DatasetScopePackage NDC
excluded productproduct
excluded packagepackage10742-1112-1
excluded packagepackage10742-1112-2
excluded packagepackage10742-1112-3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
10742-1112-12023-02-07Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-22023-02-07Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-32023-02-07Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-12023-01-30Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-22023-01-30Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-32023-01-30Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10742-1112MENTHOLATUM CHILDRENS NIGHTTIME VAPORIZING RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL) OINTMENT [THE MENTHOLATUM COMPANY]6Legacy NDC20241215_e18c434b-6d55-44f9-b500-c3a27910f7e3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10742-1112-1107421112011 JAR in 1 CARTON (10742-1112-1) > 50 g in 1 JAR1 jar2018-08-010000-00-00NoNoCurrent
10742-1112-2107421112021 JAR in 1 CARTON (10742-1112-2) > 85 g in 1 JAR1 jar2019-11-180000-00-00NoNoCurrent
10742-1112-3107421112031 JAR in 1 CARTON (10742-1112-3) > 57.5 g in 1 JAR1 jar2020-10-190000-00-00NoNoCurrent