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 4 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL	WAL-MART STORES INC	888bd90a-a059-4814-bd65-6b735ecfaf3a	2026-08-31	Warnings	Exact identifier application number: M012
Severe Cold and Flu Daytime and Nighttime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	Kroger	49a98411-aa5a-6de3-e063-6294a90a148f	2026-08-31	Warnings	Exact identifier application number: M012
equate daytime nighttime cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, GUAIFENESEN, PHENYLEPHRINE HYDROCHLORIDE	Sixarp, LLC	5a5a6917-9fb5-e6ca-e063-6394a90af9dc	2026-08-31	Warnings	Exact identifier application number: M012
Zicam Intense Sinus Relief	OXYMETAZOLINE HYDROCHLORIDE	Church & Dwight Co., Inc.	d916f7ff-84b7-57ef-e053-2995a90a3efa	2026-08-31	Warnings	Exact identifier application number: M012
Afrin Original Nasal	OXYMETAZOLINE HYDROCHLORIDE	JC World Bell Wholesale Co., Inc.	ecfa14b8-a3f3-4569-b489-c9e1a51cf09e	2026-08-31	Warnings	Exact identifier application number: M012
Dextromethorphan HBr	DEXTROMETHORPHAN HBR	BIONPHARMA INC.	5a5dde85-8785-8149-e063-6294a90a4d57	2026-08-31	Warnings	Exact identifier application number: M012
Equate Nasal	OXYMETAZOLINE HCL	Sixarp, LLC	5a5e2458-bab0-4931-e063-6394a90ad606	2026-08-31	Warnings	Exact identifier application number: M012
MUCINEX INSTASOOTHE SORE THROAT PLUS COUGH RELIEF	DEXTROMETHORPHAN HYDROBROMIDE AND HEXYLRESORCINOL	Reckitt Benckiser LLC	8d670d91-9e22-45b9-b568-5b62c2133d32	2026-08-31	Warnings	Exact identifier application number: M012
Daytime Cold and Flu Multi Symptom Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	Shield Pharmaceuticals Corp	e85b4c2a-d4e0-452c-9a08-fcc0ff6eaa21	2026-08-31	Warnings	Exact identifier application number: M012
Daytime Cold and Flu Maximum Strength	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	Shield Pharmaceuticals Corp	67849e09-2056-4013-98b1-d003ed3250a2	2026-08-31	Warnings	Exact identifier application number: M012
MAX Tussin Mucus and Chest Congestion Sugar Free	GUAIFENESIN	Akron Pharma Inc.	3b023b91-e703-4599-9864-96d8c328b45c	2026-08-31	Warnings	Exact identifier application number: M012
MAX Tussin Mucus and Chest Congestion	GUAIFENESIN	Akron Pharma Inc.	ac874a31-5556-4669-937f-dcb52aaecd8a	2026-08-31	Warnings	Exact identifier application number: M012
MAX Tussin Cough and Chest Congestion DM	DEXTROMETHORPHAN HBR, GUAIFENESIN	Akron Pharma Inc.	e0ce4287-bfa1-4413-97c8-4fe2e39bda36	2026-08-31	Warnings	Exact identifier application number: M012
Acetaminophen PM Extra Strength	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	United Natural Foods, Inc. dba UNFI	24173e77-92ec-4a87-a471-d6867837c180	2026-08-31	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	DOLGENCORP, LLC	69af44c2-390c-4223-889a-d5555aef5778	2026-08-28	Warnings	Exact identifier application number: M012
Tussin DM Daytime	DEXTROMETHORPHAN HBR, GUAIFENESIN	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	432d4833-2eaf-4f7c-b6b4-41043a6b7e2a	2026-08-28	Warnings	Exact identifier application number: M012
Chest Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Your Military Exchanges	13fcc43c-bdda-4b65-b6d7-23b39e683651	2026-08-28	Warnings, Adverse reactions	Exact identifier application number: M012
Multi-Symptom Allergy	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL	Walgreen Company	5170c450-989d-44fa-ab38-86c78feae3b6	2026-08-28	Warnings	Exact identifier application number: M012
Pain Reliever PM Extra strength	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	Walgreens	54cbbc5f-908b-47b2-b37f-3646354d3568	2026-08-27	Warnings	Exact identifier application number: M012
Maximum Strength Mucus Relief	DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Hyvee Inc	4e578c7a-88d4-e4cd-e063-6394a90aac44	2026-08-27	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