Vaporizing Chest Rub

Product NDC: 52000-039
11-digit product format: 520000039
Labeler code: 52000
Product ID: 52000-039_d8874472-8be1-38bc-e053-2995a90aaf3f
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol and Camphor and Eucalyptus Oil
Dosage form: GEL
Route: TOPICAL
Labeler: Universal Distribution Center LLC
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2018-05-14
Marketing end: 0000-00-00
Substance: CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL
Active strength: 5 g/100g; g/100g; g/100g
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 8 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	52000-039		I	Inactivated by FDA	2026-10-05
excluded package	package	52000-039	52000-039-08	I	Inactivated by FDA	2026-10-05
excluded package	package	52000-039	52000-039-09	I	Inactivated by FDA	2026-10-05
excluded package	package	52000-039	52000-039-10	I	Inactivated by FDA	2026-10-05
excluded package	package	52000-039	52000-039-11	I	Inactivated by FDA	2026-10-05
excluded package	package	52000-039	52000-039-12	I	Inactivated by FDA	2026-10-05
excluded package	package	52000-039	52000-039-13	I	Inactivated by FDA	2026-10-05
excluded package	package	52000-039	52000-039-14	I	Inactivated by FDA	2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 16 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	52000-039-08	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	52000-039-13	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	52000-039-12	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	52000-039-14	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	52000-039-09	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	52000-039-10	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	52000-039-11	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52000-039-08	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52000-039-13	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52000-039-12	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52000-039-14	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52000-039-09	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52000-039-10	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52000-039-11	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
52000-039-08	Vaporising Chest Rub
52000-039-09	Vaporising Chest Rub
52000-039-10	Vaporising Chest Rub
52000-039-11	Vaporising Chest Rub
52000-039-12	Vaporising Chest Rub
52000-039-13	Vaporising Chest Rub
52000-039-14	Vaporising Chest Rub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
52000-039-08	Vaporizing Chest Rub	50 g in 1 BOTTLE, PLASTIC	GEL	50	4
52000-039-09	Vaporizing Chest Rub	56.6 g in 1 BOTTLE, PLASTIC	GEL	56.6	4
52000-039-10	Vaporizing Chest Rub	100 g in 1 BOTTLE, PLASTIC	GEL	100	4
52000-039-11	Vaporizing Chest Rub	113 g in 1 BOTTLE, PLASTIC	GEL	113	4
52000-039-12	Vaporizing Chest Rub	150 g in 1 BOTTLE, PLASTIC	GEL	150	4
52000-039-13	Vaporizing Chest Rub	170 g in 1 BOTTLE, PLASTIC	GEL	170	4
52000-039-14	Vaporizing Chest Rub	226 g in 1 BOTTLE, PLASTIC	GEL	226	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52000-039	VAPORIZING CHEST RUB (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	4	Legacy NDC, 7 package rows	20241212_cfec7539-8db6-4bdf-9a6b-3416e9afc6d9.zip

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
2045202	camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical Gel	PSN	cfec7539-8db6-4bdf-9a6b-3416e9afc6d9	4
2045202	camphor 0.047 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.0125 MG/MG Topical Gel	SCD	cfec7539-8db6-4bdf-9a6b-3416e9afc6d9	4
2045202	camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical Gel	SY	cfec7539-8db6-4bdf-9a6b-3416e9afc6d9	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52000-039-08	52000003908	50 g in 1 BOTTLE, PLASTIC (52000-039-08)	50 g	2018-05-14	0000-00-00	No	No	Current
52000-039-09	52000003909	56.6 g in 1 BOTTLE, PLASTIC (52000-039-09)	56.6 g	2018-05-14	0000-00-00	No	No	Current
52000-039-10	52000003910	100 g in 1 BOTTLE, PLASTIC (52000-039-10)	100 g	2018-05-14	0000-00-00	No	No	Current
52000-039-11	52000003911	113 g in 1 BOTTLE, PLASTIC (52000-039-11)	113 g	2018-05-14	0000-00-00	No	No	Current
52000-039-12	52000003912	150 g in 1 BOTTLE, PLASTIC (52000-039-12)	150 g	2018-05-14	0000-00-00	No	No	Current
52000-039-13	52000003913	170 g in 1 BOTTLE, PLASTIC (52000-039-13)	170 g	2018-05-14	0000-00-00	No	No	Current
52000-039-14	52000003914	226 g in 1 BOTTLE, PLASTIC (52000-039-14)	226 g	2018-05-14	0000-00-00	No	No	Current