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 139 of 178 · 3,550 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
basic care tussin dm	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Amazon.com Services LLC	306d5914-03ed-410a-9345-c54ba604e991	2024-11-09	Warnings	Exact identifier application number: M012
care one nasal original	OXYMETAZOLINE HYDROCHLORIDE	American Sales Company	a0c35e06-c9e9-438e-8224-d4760b6e2aff	2024-11-09	Warnings	Exact identifier application number: M012
adult tussin dm	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Walgreen Company	34174507-cf2e-4ed4-85ec-f915d4b910df	2024-11-08	Warnings	Exact identifier application number: M012
Childrens Benadryl Chewables	DIPHENHYDRAMINE HYDROCHLORIDE	Kenvue Brands LLC	b08f71d8-a06c-41ba-8ed1-fbc41dbc1919	2024-11-08	Warnings	Exact identifier application number: M012
SUDAFED PE SINUS CONGESTION	DIPHENHYDRAMINE HYDROCHLORIDE AND PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	a38fdfb8-db89-487f-9b68-aa9152b91f5f	2024-11-08	Warnings	Exact identifier application number: M012
SUDAFED Sinus Congestion	PSEUDOEPHEDRINE HYDROCHLORIDE	Kenvue Brands LLC	c05d7e27-6821-468f-b27d-9c0b02a07b0f	2024-11-08	Warnings	Exact identifier application number: M012
Benadryl	DIPHENHYDRAMINE HYDROCHLORIDE	Kenvue Brands LLC	2884d2dc-2d4a-4ca6-ab73-688a80b428eb	2024-11-08	Warnings	Exact identifier application number: M012
Extra Strength TYLENOL Cold plus Flu Multi-Action Day/Night	ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, AND CHLORPHENIRAMINE MALEATE	Kenvue Brands LLC	712ba011-79aa-469b-9f0f-04a0b4b705bd	2024-11-08	Warnings	Exact identifier application number: M012
SUDAFED PE Pressure Plus Pain	ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	8538c291-9ce9-4866-b268-f4cbdb52f5bd	2024-11-08	Warnings	Exact identifier application number: M012
Childrens Sudafed Nasal Decongestant	PSEUDOEPHEDRINE HYDROCHLORIDE	Kenvue Brands LLC	52e9307b-ad38-4f65-bb2f-4fa262e82010	2024-11-08	Warnings	Exact identifier application number: M012
Benadryl Allergy Plus Congestion	DIPHENHYDRAMINE HYDROCHLORIDE AND PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	685b51d3-cc25-47b2-ac8a-368924f43137	2024-11-08	Warnings	Exact identifier application number: M012
Sudafed PE Sinus Pressure Plus Pain	ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	60183922-bfd3-4377-884a-51b2f0a4c93a	2024-11-08	Warnings	Exact identifier application number: M012
Sudafed PE Sinus Congestion	PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	2ca08917-1a75-4365-8520-c083e6a4225a	2024-11-08	Warnings	Exact identifier application number: M012
SUDAFED PE Head Congestion Plus Mucus	ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	f0739186-41b9-4761-adf7-08101b30a18e	2024-11-08	Warnings	Exact identifier application number: M012
SUDAFED PE Head Congestion Plus Flu Severe	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	1e528f78-0ced-4a06-935a-84056c921727	2024-11-08	Warnings	Exact identifier application number: M012
TYLENOL Cold Plus Flu Severe and TYLENOL COLD MAX CoPack	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	657a1e59-104c-4152-b2c9-00a8b82dc78e	2024-11-08	Warnings	Exact identifier application number: M012
Tylenol Cold plus Flu Severe and Tylenol Cold Max	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	47c61858-72ce-409b-a3af-a63620cf7d13	2024-11-08	Warnings	Exact identifier application number: M012
Childrens Benadryl Allergy Plus Congestion	DIPHENHYDRAMINE HYDROCHLORIDE AND PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	b8b75904-3806-4258-89c1-d6ff486ed41c	2024-11-08	Warnings	Exact identifier application number: M012
Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 3-Pack	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Kenvue Brands LLC	464de5de-0e7a-41d6-875f-dd0e5fe7893c	2024-11-08	Warnings	Exact identifier application number: M012
McKesson Phenylephrine HCl	PHENYLEPHRINE HCL	McKesson Medical-Surgical	e09060f7-ca0b-5f7c-e053-2995a90ab344	2024-11-08	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