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 145 of 178 · 3,550 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DAYTIME COLD AND FLU MULTI-SYMPTOM RELIEF	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE	Chain Drug Consortium, LLC	8cb0d0c8-c565-4c5a-97c5-8250a67e23a8	2024-10-24	Warnings	Exact identifier application number: M012
equate nighttime cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	Wal-Mart Stores Inc	0d07a534-c67f-4041-a07c-ed7f68dfc426	2024-10-23	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	Marc Glassman, Inc.	90977b39-8ced-46bf-9d06-15306bce9b35	2024-10-23	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	Marc Glassman, Inc.	5d29d3e3-3666-4a2f-835f-9e01bf8f5eeb	2024-10-23	Warnings	Exact identifier application number: M012
Sinus Severe	ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	MARC GLASSMAN, INC.	e2325f33-e4e4-1269-e053-2995a90ab4ac	2024-10-23	Warnings	Exact identifier application number: M012
Sinus Pressure plus Pain PE	ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE	MARC GLASSMAN, INC.	a8240d98-f0b0-3ded-e053-2a95a90a5cf9	2024-10-23	Warnings	Exact identifier application number: M012
Sinus plus Headache	ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE	MARC GLASSMAN, INC.	a82401f5-65b1-11e9-e053-2a95a90a499e	2024-10-23	Warnings	Exact identifier application number: M012
Allergy Multi Symptom	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, AND PHENYLEPHRINE HYDROCHLORIDE	MARC GLASSMAN, INC.	a823db21-4863-45a6-e053-2995a90ab8e6	2024-10-23	Warnings	Exact identifier application number: M012
Cold Max	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	MARC GLASSMAN, INC.	e2346d0c-75cf-974c-e053-2a95a90a2857	2024-10-23	Warnings	Exact identifier application number: M012
Cold Multi-Symptom Nighttime	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Marc Glassman, Inc.	ce573785-f77d-4314-9b7a-ef3f1f4f34d8	2024-10-23	Warnings	Exact identifier application number: M012
Cold plus Flu Severe	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	MARC GLASSMAN, INC.	e41a3dcc-45b4-4093-e053-2995a90a3b14	2024-10-23	Warnings	Exact identifier application number: M012
Cold plus Head Congestion Severe	ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	MARC GLASSMAN, INC.	e41a7cc5-bd0e-b92b-e053-2995a90af50a	2024-10-23	Warnings	Exact identifier application number: M012
Nighttime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	Kroger Company	1cd26a6a-4b50-4610-9fc8-278545d77f18	2024-10-23	Warnings	Exact identifier application number: M012
Nighttime Cold and Flu Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	CVS Pharmacy	c5dd40e5-b4e2-4963-9a53-b71da1ed5510	2024-10-23	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	Harris Teeter	832eb36c-21c6-46d7-b1f8-ab8b6f1e501e	2024-10-22	Warnings	Exact identifier application number: M012
Sinus plus Headache	ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE	Harris Teeter	c9d82968-b2ec-2f4b-e053-2a95a90a7f0c	2024-10-22	Warnings	Exact identifier application number: M012
Cold Max	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Harris Teeter	b9d9ab99-44b1-455f-a29a-95c193a4808e	2024-10-22	Warnings	Exact identifier application number: M012
Mucus Relief Sinus Severe Congestion and Pain	ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	HARRIS TEETER	b96c376e-578f-1124-e053-2a95a90acbb4	2024-10-22	Warnings	Exact identifier application number: M012
Tukol Honey Daytime and Nighttime Value Pack	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, AND DOXYLAMINE SUCCINATE	Genomma Lab USA	bccc11d2-d227-4cbb-b0fc-ac6abb6dce57	2024-10-22	Warnings	Exact identifier application number: M012
Cold Head Congestion Severe	ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Harris Teeter	c92b508b-e5f9-4149-8c4b-d21845943b3b	2024-10-22	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