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 81 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Basic Care Honey Lemon Cough Drops	MENTHOL	Amazon.com	c0937b13-f679-a764-e053-2a95a90abf89	2025-12-05	Warnings	Exact identifier application number: M012
Basic Care SF Menthol Cough Drops	MENTHOL	Amazon.com	c0946295-7cf0-1bd8-e053-2a95a90af5af	2025-12-05	Warnings	Exact identifier application number: M012
Basic Care SF Honey Lemon Cough Drops	MENTHOL	Amazon.com	cf82fb0b-1b4d-def1-e053-2995a90a6fd9	2025-12-05	Warnings	Exact identifier application number: M012
G-DOLOGEN	ACETAMINOPHEN, DEXBROMPHENIRAMINE MALEATE	Kramer Novis	7a4e1d64-2510-405f-a1dc-e02a803b6fbd	2025-12-05	Warnings	Exact identifier application number: M012
Quality Choice Severe Cold and Cough Nighttime	ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE	Chain Drug Manufacturing Assn	ce658dd5-b683-436e-b16b-0c06f6f87fd9	2025-12-04	Warnings	Exact identifier application number: M012
Quality Choice Maximum Strength	OXYMETAZOLINE HYDROCHLORIDE	CHAIN DRUG MARKETING ASSOCIATION	a87ba15f-b5a9-4983-a721-ca7f705aea86	2025-12-04	Warnings	Exact identifier application number: M012
Quality Choice	PHENYLEPHRINE HYDROCHLORIDE	CHAIN DRUG MARKETING ASSOCIATION	a12e2e66-d2f3-47a6-a915-a309ae828d27	2025-12-04	Warnings	Exact identifier application number: M012
Childrens Mucus Relief Chest Congestion	GUAIFENESIN	Chain Drug Manufacturing Assn	034d39c0-9aad-4dff-a158-a041b9f0504f	2025-12-04	Warnings	Exact identifier application number: M012
Quality Choice	OXYMETAZOLINE HYDROCHLORIDE	CHAIN DRUG MARKETING ASSOCIATION	d01b8fb6-1ddf-4901-bda6-ae608e94a6a4	2025-12-04	Warnings	Exact identifier application number: M012
Childrens Mucus and Cough Relief	GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE	Chain Drug Manufacturing Assn	06822a28-3f82-471d-8db5-c5981b263a03	2025-12-04	Warnings	Exact identifier application number: M012
QUALITY CHOICE	PHENYLEPHRINE HYDROCHLORIDE	CHAIN DRUG MARKETING ASSOCIATION	14596551-dd82-46b3-8eb8-e69efaea105b	2025-12-04	Warnings	Exact identifier application number: M012
Daytime Cold and Flu Lil Drug Store Products	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Lil' Drug Store Products, Inc	fd5c20ed-5520-4db0-bfd4-995f043af2a4	2025-12-04	Warnings	Exact identifier application number: M012
Afrin Original	OXYMETAZOLINE HYDROCHLORIDE	Bayer HealthCare LLC.	89c165ba-3ad5-49b5-a5bb-423dc8e15bad	2025-12-04	Warnings	Exact identifier application number: M012
Alka-Seltzer Plus Severe Cold Powerfast Fizz Night	ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE BITARTRATE	Bayer HealthCare LLC.	a2b30c27-b836-f09f-e053-2995a90ac383	2025-12-04	Warnings	Exact identifier application number: M012
Alka-Seltzer Plus Severe Cold PowerFast Fizz	ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE, DOXYLAMINE SUCCINATE	Bayer HealthCare LLC.	a37c9d9d-52db-23ff-e053-2995a90a8f76	2025-12-04	Warnings	Exact identifier application number: M012
Alka-Seltzer Plus Severe Cold and Cough PowerFast Fizz	ASPIRIN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE	Bayer Healthcare LLC.	dd7d8a8c-0f91-5ef1-e053-2a95a90a3c6a	2025-12-04	Warnings	Exact identifier application number: M012
Alka-Seltzer Plus Cough, Mucus and Congestion Day and Night Powermax	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Bayer HealthCare LLC.	a68df74d-dd26-3ae9-e053-2995a90a08d6	2025-12-04	Warnings	Exact identifier application number: M012
Circle K Daytime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Lil' Drug Store Products, Inc.	55662ada-677e-4048-9529-5bca44076316	2025-12-04	Warnings	Exact identifier application number: M012
Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu	DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE	Bayer HealthCare LLC.	b13d5132-cb91-3cf6-e053-2a95a90aa47c	2025-12-04	Warnings	Exact identifier application number: M012
Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz	CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE	Bayer HealthCare LLC.	bd97e91f-1ae1-379c-e053-2995a90acfdd	2025-12-04	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