Bronco Rub

Product NDC: 66513-220
11-digit product format: 665130220
Labeler code: 66513
Product ID: 66513-220_eb017336-7b4d-7039-e053-2995a90a6a2c
Type: HUMAN OTC DRUG
Nonproprietary name: Camphor Eucalyptus Menthol
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Distribuidora de Alimentos Naturales y Nutricionales, S.A. de C.V
Application: M012
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2014-08-15
Marketing end: 0000-00-00
Substance: CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL
Active strength: 5 g/100g; g/100g; g/100g
NDC exclude flag: No
Listing certified through: 2023-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	66513-220		D	Discontinued by firm		2026-10-23
excluded package	package	66513-220	66513-220-14	D	Discontinued by firm		2026-10-23

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 · 22 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	66513-220-14	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	66513-220-14	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	66513-220-14	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	66513-220-14	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	66513-220-14	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	66513-220-14	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	66513-220-14	`302b2466d912…`	`e7b80fea0513…`
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	66513-220-14	`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	66513-220-14	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	66513-220-14	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	66513-220-14	`367a005e9d99…`	`383a685ebd0f…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	BRONCO RUB (CAMPHOR EUCALYPTUS MENTHOL) OINTMENT [DISTRIBUIDORA DE ALIMENTOS NATURALES Y NUTRICIONALES, S.A. DE C.V]	1
EUCALYPTUS OIL	ACTIVE INGREDIENT	2R04ONI662	BRONCO RUB (CAMPHOR EUCALYPTUS MENTHOL) OINTMENT [DISTRIBUIDORA DE ALIMENTOS NATURALES Y NUTRICIONALES, S.A. DE C.V]	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	BRONCO RUB (CAMPHOR EUCALYPTUS MENTHOL) OINTMENT [DISTRIBUIDORA DE ALIMENTOS NATURALES Y NUTRICIONALES, S.A. DE C.V]	1
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	BRONCO RUB (CAMPHOR EUCALYPTUS MENTHOL) OINTMENT [DISTRIBUIDORA DE ALIMENTOS NATURALES Y NUTRICIONALES, S.A. DE C.V]	1
EUCALYPTUS OIL	ACTIVE MOIETY	2R04ONI662	BRONCO RUB (CAMPHOR EUCALYPTUS MENTHOL) OINTMENT [DISTRIBUIDORA DE ALIMENTOS NATURALES Y NUTRICIONALES, S.A. DE C.V]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	BRONCO RUB (CAMPHOR EUCALYPTUS MENTHOL) OINTMENT [DISTRIBUIDORA DE ALIMENTOS NATURALES Y NUTRICIONALES, S.A. DE C.V]	1
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	BRONCO RUB (CAMPHOR EUCALYPTUS MENTHOL) OINTMENT [DISTRIBUIDORA DE ALIMENTOS NATURALES Y NUTRICIONALES, S.A. DE C.V]	1
TURPENTINE OIL	INACTIVE INGREDIENT	C5H0QJ6V7F	BRONCO RUB (CAMPHOR EUCALYPTUS MENTHOL) OINTMENT [DISTRIBUIDORA DE ALIMENTOS NATURALES Y NUTRICIONALES, S.A. DE C.V]	1

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 109 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Viva Porru Chest Rub	CAMPHOR, MENTHOL, EUCALYPTUS OIL	Menper Distributors, Inc.	0dfadfe3-9e40-0eee-e063-6294a90a00c3	2025-07-22	Warnings	Exact identifier application number: M012
leader childrens allergy relief	DIPHENHYDRAMINE HCL	Cardinal Health 110, LLC. dba Leader	40d697b7-dc59-4d24-8d46-db635e01b9d5	2025-07-22	Warnings	Exact identifier application number: M012
Allergy Relief	CHLORPHENIRAMINE MALEATE	Chain Drug Consortium	34005c55-3176-4f28-9a3b-7dc6fefd01fe	2025-07-19	Warnings	Exact identifier application number: M012
Sinus Relief Daytime Nighttime	ACETAMINOPHEN, DIPHENHYDRAMINE HCL, GUAIFENESIN, PHENYLEPHRINE HCL	Kroger Company	73a77a13-983b-4e65-bb3c-2ba5e9f33a3e	2025-07-19	Warnings	Exact identifier application number: M012
QUALITY CHOICE No Drip Nasal Mist	OXYMETAZOLINE HYDROCHLORIDE	QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)	7cb6ad04-7847-46b9-b371-0a3473001c79	2025-07-18	Warnings	Exact identifier application number: M012
Nasal Decongestant Maximum Strength	PSEUDOEPHEDRINE HCL	Chain Drug Consortium	270e9221-d305-4148-b523-741e02fe733f	2025-07-18	Warnings	Exact identifier application number: M012
ACTISPEC PSE	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE	ACTIPHARMA, LLC	5def1555-87f4-41d5-8a5c-be560aa8f1e2	2025-07-17	Warnings	Exact identifier application number: M012
EXTRA STRENGTH TYLENOL SEVERE COUGH PLUS SORE THROAT DAY	ACETAMINOPHEN AND DEXTROMETHORPHAN HYDROBROMIDE	Kenvue Brands LLC	1a17b24a-8022-4e2f-e063-6294a90af276	2025-07-17	Warnings	Exact identifier application number: M012
BULPOL Smoking Patches	MENTHOL	Jiashen International Trade Limited	3a1cc0e1-fabf-52b9-e063-6394a90ae35e	2025-07-17	Warnings	Exact identifier application number: M012
Ampigrin Ultra Forte Night	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	OPMX LLC	e11e71c3-fe7c-77c7-e053-2995a90a34b2	2025-07-17	Warnings	Exact identifier application number: M012
Nitecin	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	OPMX LLC	dfb56532-6f72-1e4d-e053-2a95a90a1c05	2025-07-17	Warnings	Exact identifier application number: M012
tabcin NIGHT	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	OPMX LLC	0b3ed2bb-88ed-699e-e063-6394a90ac023	2025-07-17	Warnings	Exact identifier application number: M012
Pentrexcilina Night Time	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	OPMX LLC	e11e5c17-28f2-7186-e053-2995a90a51f6	2025-07-17	Warnings	Exact identifier application number: M012
Viro Flu PM Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	OPMX LLC	e1553da8-3a89-e258-e053-2a95a90a4725	2025-07-17	Warnings	Exact identifier application number: M012
ACTICON PEDIATRIC	DEXBROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE	ACTIPHARMA, LLC	3052cc67-e6c0-4d3f-9ec9-ffe58d9fae23	2025-07-17	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	Demoulas Super Markets, Inc	397f5acd-31c0-683e-e063-6394a90a7e54	2025-07-16	Warnings	Exact identifier application number: M012
EXTRA STRENGTH TYLENOL SEVERE COUGH PLUS SORE THROAT DAY/NIGHT	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE	Kenvue Brands LLC	19ad2cca-c1cb-019c-e063-6294a90a5644	2025-07-16	Warnings	Exact identifier application number: M012
DG HEALTH COLD FLU RELIEF	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	Dolgencorp Inc	8ea03891-2fbc-4413-8e6d-de903d426f8d	2025-07-16	Warnings	Exact identifier application number: M012
up and up nighttime flu and severe cold and cough	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Target Corporation	df488727-b913-440b-9a0b-cce3ae143bf2	2025-07-15	Warnings	Exact identifier application number: M012
Topcare DayTime Cold and Flu Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE	Topco Associates LLC	bb9663e3-fd11-4e72-bf85-fee4841b795f	2025-07-15	Warnings	Exact identifier application number: M012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)
2R04ONI662	EUCALYPTUS OIL	8000-48-4	EUCALYPTUS OIL

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66513-220-14	66513022014	39 g in 1 JAR (66513-220-14)	39 g	2014-08-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Bronco Rub - Distribuidora de Alimentos Naturales y Nutricionales, S.A. de C.V	Distribuidora de Alimentos Naturales y Nutricionales, S.A. de C.V	2022-10-14	HUMAN OTC DRUG LABEL	3