Mentholatum Childrens Nighttime Vaporizing Rub

Product NDC: 10742-1112
Requested package NDC: 10742-1112-3
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	10742-1112	10742-1112-3	D	Discontinued by firm		2026-10-05

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 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	10742-1112	10742-1112-3	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`

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
NDC	Effective	Related label
10742-1112-1	2023-02-07	Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-2	2023-02-07	Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-3	2023-02-07	Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-1	2023-01-30	Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-2	2023-01-30	Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub
10742-1112-3	2023-01-30	Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10742-1112	MENTHOLATUM CHILDRENS NIGHTTIME VAPORIZING RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL) OINTMENT [THE MENTHOLATUM COMPANY]	6	Legacy NDC	20241215_e18c434b-6d55-44f9-b500-c3a27910f7e3.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
N20HL7Q941	CAMPHOR (NATURAL)	464-49-3	CAMPHOR (NATURAL)
2R04ONI662	EUCALYPTUS OIL	8000-48-4	EUCALYPTUS OIL
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
10742-1112-3	10742111203	1 JAR in 1 CARTON (10742-1112-3) > 57.5 g in 1 JAR	1 jar	2020-10-19	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts - Mentholatum Childrens Nighttime Vaporizing Rub	The Mentholatum Company	2024-12-13	HUMAN OTC DRUG LABEL	6