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 173 of 177 · 3,534 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Akin	GUAIFENESIN	Southern Sales & Service, Inc.	bb2c9f21-6765-4286-bd71-de01cdf4c4e9	2023-11-29	Warnings	Exact identifier application number: M012
Akin Cough Formula DM	DEXTROMETHORPHAN, GUAIFENESIN	Southern Sales & Service, Inc.	1f2f9b4c-ecf0-4ff6-861a-063f8a9ef74a	2023-11-29	Warnings	Exact identifier application number: M012
diphenhydramine hydrochloride	DIPHENHYDRAMINE HYDROCHLORIDE	Simpex Pharma Pvt. Ltd	82771f6a-8b3d-4ffa-8b35-09c2faf3582c	2023-11-29	Warnings	Exact identifier application number: M012
SIMPEX Guaifenesin	GUAIFENESIN	Simpex Pharma Pvt. Ltd	1594f9d6-0c48-42bf-b76b-d621f215179a	2023-11-29	Warnings	Exact identifier application number: M012
Stona	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE	Sato Pharmaceutical Co., Ltd.	8b89f50d-88f8-4773-92ea-5ada61766056	2023-11-28	Warnings	Exact identifier application number: M012
Stona	DEXTROMETHORPHAN HYDROBROMIDE	Sato Pharmaceutical Co., Ltd.	1ccc9e56-32a4-450f-8412-5814b6aef285	2023-11-28	Warnings	Exact identifier application number: M012
Neo-Synephrine Maximum	PHENYLEPHRINE HYDROCHLORIDE	BF ASCHER AND CO INC	ab8682a4-1f66-6709-e053-2995a90a8b4a	2023-11-16	Warnings	Exact identifier application number: M012
Neo-Synephrine Regular	PHENYLEPHRINE HYDROCHLORIDE	BF ASCHER AND CO INC	ab860c10-b8cf-3f92-e053-2a95a90a7317	2023-11-16	Warnings	Exact identifier application number: M012
Neo-Synephrine Mild	PHENYLEPHRINE HYDROCHLORIDE	BF ASCHER AND CO INC	9b8e9162-e4da-14d9-e053-2995a90a2269	2023-11-16	Warnings	Exact identifier application number: M012
Universal Vaporizing Chest Rub	MENTHOL AND CAMPHOR AND EUCALYPTUS	Universal Distribution Center LLC	b1d25572-da21-408d-aab3-3a0741dfff12	2023-11-16	Warnings	Exact identifier application number: M012
Daytime Cold and Flu Severe, Caseys 4goog	ACETAMINOPHEN, PHENYLEPHRINE, DEXTROMETHORPHAN HBR, GUAIFENESIN TABLET, FILM COATED	Lil' Drug Store Products, Inc.	0334259d-587e-b2d5-e063-6394a90a3e56	2023-11-14	Warnings	Exact identifier application number: M012
Stona Cough	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	Sato Pharmaceutical Co., Ltd.	0b638db4-5ed3-4665-abcd-f95e677adbd8	2023-11-12	Warnings	Exact identifier application number: M012
Tylenol Sinus Severe	ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Jones Healthcare Group - Packaging Services, Inc	6c90b415-4c5f-49e5-beb6-4cf225797b21	2023-11-06	Warnings	Exact identifier application number: M012
Tylenol Cold Plus Flu Severe Severe	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Jones Healthcare Group - Packaging Services, Inc	8b8582c0-8aef-482f-9738-2f1d4e325d64	2023-11-06	Warnings	Exact identifier application number: M012
Cold and Flu Severe Daytime/Nighttime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE	Topco Associates LLC	27ade5f8-2003-4dc6-9244-42676791e1f8	2023-11-06	Warnings	Exact identifier application number: M012
Benadryl Allergy Ultratab	DIPHENHYDRAMINE HYDROCHLORIDE	Jones Healthcare Group - Packaging Services, Inc	ec2070df-8a8a-4cd1-8830-62655433fb3b	2023-11-05	Warnings	Exact identifier application number: M012
Daytime Nighttime Ultra Concentrated Cold and Flu	DAYTIME - ACETAMINOPHEN, DEXTROMETHROPHAN HBR AND NIGHTTIME - ACETAMINOPHEN, DEXTROMETHROPHAN HBR, DOXYLAMINE SUCCINATE	TARGET CORPORATION	093eed84-79b1-7914-e063-6394a90a37af	2023-11-03	Warnings	Exact identifier application number: M012
Cough Drops	MENTHOL	Topco Associates LLC	eff68377-2273-6c6c-e053-2995a90a36b2	2023-11-03	Warnings	Exact identifier application number: M012
Sugar Free Cough Drops	MENTHOL	Topco Associates LLC	096bbcaa-fce1-0fc2-e063-6294a90ad597	2023-11-03	Warnings	Exact identifier application number: M012
TopCare Nite Time SEVERE Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE	Topco Associates LLC	adc8edf5-ebbe-4d94-9018-aa0dbe118112	2023-11-03	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