Chestrub

Product NDC: 20276-100
11-digit product format: 202760100
Labeler code: 20276
Product ID: 20276-100_29740204-fdf3-705b-e063-6294a90a0acf
Type: HUMAN OTC DRUG
Nonproprietary name: Camphor Menthol Eucalyptus Oil
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Delta Brands Inc
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2009-11-15
Substance: CAMPHOR (SYNTHETIC); MENTHOL; EUCALYPTUS OIL
Active strength: 4.7; 1; 1 g/100g; g/100g; g/100g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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: Chestrub
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	4.7 g/100g
MENTHOL	1 g/100g
EUCALYPTUS OIL	1 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
1042786	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
8e6f731f-c16a-41b2-9786-0cab588cfc8e	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
20276-100-31	Chestrub	113 g in 1 JAR	OINTMENT	113		6

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
EUCALYPTUS OIL	ACTIVE INGREDIENT	2R04ONI662	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
EUCALYPTUS OIL	ACTIVE MOIETY	2R04ONI662	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
CEDAR LEAF OIL	INACTIVE INGREDIENT	BJ169U4NLG	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
NUTMEG	INACTIVE INGREDIENT	AEE24M3MQ9	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
PARAFFIN	INACTIVE INGREDIENT	I9O0E3H2ZE	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
THYMOL	INACTIVE INGREDIENT	3J50XA376E	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3
TURPENTINE	INACTIVE INGREDIENT	XJ6RUH0O4G	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL ) OINTMENT [DELTA BRANDS INC]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
20276-100	CHESTRUB (CAMPHOR MENTHOL EUCALYPTUS OIL) OINTMENT [DELTA BRANDS INC]	6	Current NDC, Legacy NDC, 1 package rows	20241219_8e6f731f-c16a-41b2-9786-0cab588cfc8e.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 155 of 177 · 3,534 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Topcare Nasal	OXYMETAZOLINE HYDROCHLORIDE	Topco Associates LLC	f1dd78e0-f700-4469-85d6-18cc299e8746	2024-08-28	Warnings	Exact identifier application number: M012
equaline nasal	OXYMETAZOLINE HCL	United Natural Foods, Inc. dba UNFI	69308693-a094-42a9-a041-e73647a25cc1	2024-08-27	Warnings	Exact identifier application number: M012
signature care nasal decongestant	OXYMETAZOLINE HYDROCHLORIDE	Safeway	f9ac80d1-3753-412b-a407-18a6b50e5d1c	2024-08-27	Warnings	Exact identifier application number: M012
Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu PowerMax Gels	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE	Bayer HealthCare LLC.	20ac6010-84f4-eeff-e063-6294a90a50a7	2024-08-27	Warnings	Exact identifier application number: M012
Exchange Select Nasal	OXYMETAZOLINE HCL	Army & Air Force Exchange Service	40d2090d-c332-4dcb-9f43-5ee467e7b3d1	2024-08-27	Warnings	Exact identifier application number: M012
Signature Care Nasal Decongestant	OXYMETAZOLINE HCL	Safeway	23f0a5b3-59ae-4eb3-9b7d-e6a492060337	2024-08-27	Warnings	Exact identifier application number: M012
DG Health Nasal	OXYMETAZOLINE HYDROCHLORIDE	Dolgencorp, LLC	debcda99-c605-4941-b873-9e4dbae27483	2024-08-27	Warnings	Exact identifier application number: M012
Good Neighbor Pharmacy Nasal	OXYMETAZOLINE HCL	Amerisource Bergen	d374d697-2b57-4558-a20b-d3d89aea82d7	2024-08-27	Warnings	Exact identifier application number: M012
nasal	OXYMETAZOLINE HCL	Meijer Distribution Inc	3984cbc3-b60c-40a7-bc3a-7d1f600503ac	2024-08-27	Warnings	Exact identifier application number: M012
foster and thrive nasal	OXYMETAZOLINE HYDROCHLORIDE	Strategic Sourcing Services LLC	e6e51821-03ae-4ec3-82a9-b4a8feacd996	2024-08-27	Warnings	Exact identifier application number: M012
Pyrilamine Maleate and Dextromethorphan Hydrobromide	PYRILAMINE MALEATE AND DEXTROMETHORPHAN HYDROBROMIDE	Westminster Pharmaceuticals, LLC	dd068449-9d24-41e6-8a6e-f69c9fe263f2	2024-08-26	Warnings	Exact identifier application number: M012
basic care nasal	OXYMETAZOLINE HYDROCHLORIDE	Amazon.com Services LLC	a154e500-2b45-4242-a26c-9530849f99df	2024-08-23	Warnings	Exact identifier application number: M012
Daytime Nighttime Ultra Concentrated Cold and Flu	DAYTIME - ACETAMINOPHEN, DEXTROMETHROPHAN HBR, PHENYLEPHRINE HCL AND NIGHTTIME - ACETAMINOPHEN, DEXTROMETHROPHAN HBR, DOXYLAMINE SUCCINATE	TARGET CORPORATION	0c0cf76f-2dd3-45ef-e063-6394a90a9fef	2024-08-22	Warnings	Exact identifier application number: M012
Day Cold and Flu and Night Severe Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, TRIPROLIDINE HCL	TARGET CORPORATION	08ee56d1-b11d-3e36-e063-6294a90acd5f	2024-08-22	Warnings	Exact identifier application number: M012
Maximum Strength Daytime Cold and Flu and Nighttime Severe Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, AND ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE,TRIPROLIDINE HYDROCHLORIDE	TARGET CORPORATION	0fc523ce-55a7-6384-e063-6394a90aad3f	2024-08-22	Warnings	Exact identifier application number: M012
Cold and Flu Nighttime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	Walgreens	8045aef9-22bc-4146-b494-dbb1ffef06df	2024-08-19	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	CHAIN DRUG MARKETING ASSOCIATION, INC.	5a2053d4-9c0d-4613-9cf5-0067173f3730	2024-08-16	Warnings	Exact identifier application number: M012
QUALITY CHOICE Long Acting Cough Softgel	DEXTROMETHORPHAN HYDROBROMIDE	Chain Drug Marketing Association, Inc.	f1ea7dfc-c605-45a1-ad1d-6e636a8a7b1c	2024-08-16	Warnings	Exact identifier application number: M012
pseudoephedrine hydrochloride	PSEUDOEPHEDRINE HCL	Padagis Israel Pharmaceuticals Ltd	458594e1-8d99-4de3-8923-2fd8ce2fc406	2024-08-16	Warnings	Exact identifier application number: M012
Halls Sugar Free Mountain Menthol	MENTHOL	Mondelez Global LLC	54e0d57e-1f48-45e2-86b3-0e50775996f4	2024-08-15	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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1042786	camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Ointment	PSN	8e6f731f-c16a-41b2-9786-0cab588cfc8e	6
1042786	camphor 0.047 MG/MG / Eucalyptus oil 0.01 MG/MG / menthol 0.01 MG/MG Topical Ointment	SCD	8e6f731f-c16a-41b2-9786-0cab588cfc8e	6
1042786	camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Ointment	SY	8e6f731f-c16a-41b2-9786-0cab588cfc8e	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
20276-100-31	20276010031	113 g in 1 JAR (20276-100-31)	113 g	2009-11-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Chestrub - Delta Brands Inc \| JELL PHARMACEUTICALS PVT LTD	Delta Brands Inc \| JELL PHARMACEUTICALS PVT LTD	2024-12-17	HUMAN OTC DRUG LABEL	6