Chest Rub

Product NDC: 52920-133
11-digit product format: 529200133
Labeler code: 52920
Product ID: 52920-133_299b2029-a2c9-dae0-e063-6294a90a1040
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol and Camphor and Eucalyptus Oil
Dosage form: GEL
Route: TOPICAL
Labeler: Singhfam Corporation
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-08-10
Substance: CAMPHOR (SYNTHETIC); MENTHOL; EUCALYPTUS OIL
Active strength: 4.8; 2.6; 1.2 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, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	52920-133-48	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	52920-133-48	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	52920-133-48	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	52920-133-48	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	52920-133-48	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	52920-133-48	`9bebd1f3094a…`	`5416666fcb17…`

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: Chest Rub
Brand name suffix: Vaporizing Action
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	4.8 g/100g
MENTHOL	2.6 g/100g
EUCALYPTUS OIL	1.2 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
L7T10EIP3A	Internal UNII lookup
2R04ONI662	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1547992	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
c6ea663a-9c4f-4d1a-a937-002806a8530a	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52920-133-48	2022-11-21	C162847	48780-1	9d75b9d0-d090-f424-e053-dadaa90a57ce	c6ea663a-9c4f-4d1a-a937-002806a8530a
52920-133-48	2020-01-31	C162847	48780-1	9d75b9d0-d090-f424-e053-dadaa90a57ce	c6ea663a-9c4f-4d1a-a937-002806a8530a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52920-133-48	Chest RubVaporizing Action	113 g in 1 BOTTLE, PLASTIC	GEL	113		4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
EUCALYPTUS OIL	ACTIVE INGREDIENT	2R04ONI662	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
EUCALYPTUS OIL	ACTIVE MOIETY	2R04ONI662	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
CEDAR LEAF OIL	INACTIVE INGREDIENT	BJ169U4NLG	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
NUTMEG OIL	INACTIVE INGREDIENT	Z1CLM48948	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
PARAFFIN	INACTIVE INGREDIENT	I9O0E3H2ZE	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
THYMOL	INACTIVE INGREDIENT	3J50XA376E	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1
TURPENTINE OIL	INACTIVE INGREDIENT	C5H0QJ6V7F	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52920-133	CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]	4	Current NDC, Legacy NDC, 1 package rows	20241222_c6ea663a-9c4f-4d1a-a937-002806a8530a.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 83 of 178 · 3,550 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Afrin No Drip Pump Mist Bundle Pack	OXYMETAZOLINE HYDROCHLORIDE	Bayer HealthCare LLC.	16c52c79-baec-87db-e063-6294a90a3b3b	2025-12-04	Warnings	Exact identifier application number: M012
Afrin Original Pump Mist	OXYMETAZOLINE HYDROCHLORIDE	Bayer HealthCare LLC.	0f5ec576-f788-40aa-9088-0dd672e3cc7c	2025-12-04	Warnings	Exact identifier application number: M012
Adult Long Lasting Cough Relief	DEXTROMETHORPHAN HBR	Shield Pharmaceuticals Corp	432a79a9-c69d-4514-894a-7832e1b745ef	2025-12-04	Warnings	Exact identifier application number: M012
GENCONTUSS	CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE	KRAMER NOVIS	69d16d25-b09b-430e-8e01-0962d840dc21	2025-12-04	Warnings	Exact identifier application number: M012
Nasal Decongestant PE	PHENYLEPHRINE HCL	H E B	7c04ab14-af28-4598-90ef-56ac11902c7d	2025-12-04	Warnings	Exact identifier application number: M012
Desgen Pediatric	DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL	Kramer Novis	12425c1b-8bdc-446b-83dd-95e05a4d9b8c	2025-12-04	Warnings	Exact identifier application number: M012
Presgen B	DEXTROMETHORPHAN HYDROBROMIDE, BROMPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE	KRAMER NOVIS	5befa829-32bd-4978-8a0e-1d6513ff37a4	2025-12-03	Warnings	Exact identifier application number: M012
TUSSLIN	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Kramer Novis	987e19a5-032f-44e9-b4c7-8a764d502695	2025-12-03	Warnings	Exact identifier application number: M012
DayTime Relief, Cold and Flu, 24-7 Life by 7-Eleven	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL SOLUTION	Lil' Drug Store Products, Inc.	450e8974-8ff8-4b82-e063-6394a90a9366	2025-12-03	Warnings	Exact identifier application number: M012
Nighttime Relief, Cold and Flu, 24-7 Life by 7-Eleven	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE SOLUTION	Lil' Drug Store Products, Inc.	4510223f-1c88-2796-e063-6394a90a18ac	2025-12-03	Warnings	Exact identifier application number: M012
Carolina Crud Crusher	DEXTROMETHORPHAN HBR, GUAIFENESIN	Weeks & Leo Co., Inc.	0b606683-7d68-cca5-e063-6394a90a6f58	2025-12-03	Warnings	Exact identifier application number: M012
Capmist DM	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE	Capital Pharmaceutical, LLC	63733ac3-859e-4a8e-8717-d852bd303408	2025-12-03	Warnings	Exact identifier application number: M012
ALA-HIST IR	DEXBROMPHENIRAMINE MALEATE	Poly Pharmaceuticals, Inc.	0d203b5c-8b10-428b-8703-17be6b4ce6eb	2025-12-03	Warnings	Exact identifier application number: M012
ALAHIST DM	DEXTROMETHORPHAN HBR, PHENIRAMINE MALEATE, PHENYLEPHRINE HCL	Poly Pharmaceuticals, Inc.	fdaa062d-110e-798d-e053-6394a90a755c	2025-12-03	Warnings	Exact identifier application number: M012
Alahist D	PHENIRAMINE MALEATE, PHENYLEPHRINE HCL	Poly Pharmaceuticals, Inc.	a1b8533a-ef8b-57cc-e053-2995a90a5d9e	2025-12-03	Warnings	Exact identifier application number: M012
Alahist PE	DEXBROMPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE	Poly Pharmaceuticals, Inc.	ada2d582-5813-2029-e053-2a95a90ae567	2025-12-03	Warnings	Exact identifier application number: M012
Benadryl Allergy Extra Strength Liqui-Gels	DIPHENHYDRAMINE HYDROCHLORIDE	Kenvue Brands LLC	30aca3ab-b091-3939-e063-6294a90a9819	2025-12-03	Warnings	Exact identifier application number: M012
Cough and Cold HBP	CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR	L.N.K. International, Inc.	9f2daffc-1904-4d64-9f84-689c88601e06	2025-12-03	Warnings	Exact identifier application number: M012
Childrens Multi-symptom Cold	DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Wal-Mart Stores, Inc.	d291faa9-894e-421c-8115-8a8c2a937172	2025-12-03	Warnings	Exact identifier application number: M012
SINUS PAIN AND CONGESTION	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL	CVS Pharmacy	697dffdd-5b56-4395-8e69-6b4360d9fdc5	2025-12-02	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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1547992	camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Gel	PSN	c6ea663a-9c4f-4d1a-a937-002806a8530a	4
1547992	camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical Gel	SCD	c6ea663a-9c4f-4d1a-a937-002806a8530a	4
1547992	camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Gel	SY	c6ea663a-9c4f-4d1a-a937-002806a8530a	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52920-133-48	52920013348	113 g in 1 BOTTLE, PLASTIC (52920-133-48)	113 g	2022-11-21	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
PETROLATUM - Singhfam Corporation \| Jell Pharmaceuticals Pvt. Ltd.	Singhfam Corporation \| Jell Pharmaceuticals Pvt. Ltd.	2024-12-19	HUMAN OTC DRUG LABEL	4