FDA.reportPublic FDA data

Chest Rub

Product NDC
52920-133
11-digit product format
529200133
Labeler code
52920
Product ID
52920-133_299b2029-a2c9-dae0-e063-6294a90a1040
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol and Camphor and Eucalyptus Oil
Dosage form
GEL
Route
TOPICAL
Labeler
Singhfam Corporation
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2015-08-10
Substance
CAMPHOR (SYNTHETIC); MENTHOL; EUCALYPTUS OIL
Active strength
4.8; 2.6; 1.2 g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

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 · 12 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage52920-133-48fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproduct86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage52920-133-4886f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage52920-133-48bd6a592717d7…303034d00443…
2021-12-27 23:28 UTC · source 2021-12-27excluded productproduct8dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage52920-133-488dfbde2a14a4…c9ff85d89658…
2020-12-18 03:04 UTC · source 2020-12-17excluded productproducte2bbac7714bc…27bdfed8d636…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage52920-133-48e2bbac7714bc…27bdfed8d636…
2020-06-10 20:45 UTC · source 2020-06-10excluded productproduct9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage52920-133-489bebd1f3094a…5416666fcb17…

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
Chest Rub
Brand name suffix
Vaporizing Action
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAMPHOR (SYNTHETIC)4.8 g/100g
MENTHOL2.6 g/100g
EUCALYPTUS OIL1.2 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5TJD82A1ETInternal UNII lookup
L7T10EIP3AInternal UNII lookup
2R04ONI662Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1547992Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
c6ea663a-9c4f-4d1a-a937-002806a8530aAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52920-133-482022-11-21C16284748780-19d75b9d0-d090-f424-e053-dadaa90a57cec6ea663a-9c4f-4d1a-a937-002806a8530a
52920-133-482020-01-31C16284748780-19d75b9d0-d090-f424-e053-dadaa90a57cec6ea663a-9c4f-4d1a-a937-002806a8530a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52920-133-48Chest RubVaporizing Action113 g in 1 BOTTLE, PLASTICGEL1134

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ETCHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
EUCALYPTUS OILACTIVE INGREDIENT2R04ONI662CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
MENTHOLACTIVE INGREDIENTL7T10EIP3ACHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ETCHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
EUCALYPTUS OILACTIVE MOIETY2R04ONI662CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
MENTHOLACTIVE MOIETYL7T10EIP3ACHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
CEDAR LEAF OILINACTIVE INGREDIENTBJ169U4NLGCHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
NUTMEG OILINACTIVE INGREDIENTZ1CLM48948CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
PARAFFININACTIVE INGREDIENTI9O0E3H2ZECHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
PETROLATUMINACTIVE INGREDIENT4T6H12BN9UCHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
THYMOLINACTIVE INGREDIENT3J50XA376ECHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1
TURPENTINE OILINACTIVE INGREDIENTC5H0QJ6V7FCHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52920-133CHEST RUB VAPORIZING ACTION (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [SINGHFAM CORPORATION]4Current NDC, Legacy NDC, 1 package rows20241222_c6ea663a-9c4f-4d1a-a937-002806a8530a.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 31 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MUCINEX Rapid Clear Day Night and Clear and Cool NasalACETAMINOPHEN, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, TRIPROLIDINE HYDROCHLORIDE, AND OXYMETAZOLINE HYDROCHLORIDEReckitt Benckiser LLC37dcb0ed-df56-1bec-e063-6394a90a695e2026-05-13WarningsExact identifier
application number: M012
Mucinex Rapid Clear Pain, Headache, and Mucus Congestion and Sinus Max Clear and CoolOXYMETAZOLINE HYDROCHLORIDE, ACETAMINOPHEN AND GUAIFENESINReckitt Benckiser LLC373e0d75-8def-4b98-e063-6394a90a5e472026-05-13WarningsExact identifier
application number: M012
MUCINEX SINUS-MAX SEVERE NASAL CONGESTION RELIEF CLEAR and COOL NASALOXYMETAZOLINE HYDROCHLORIDEReckitt Benckiser LLC5a397466-8721-4060-a178-5ebfd7069cc92026-05-13WarningsExact identifier
application number: M012
Maximum Strength Mucinex Sinus-Max Pressure, Pain and CoughACETAMINOPHEN, GUAIFENESINReckitt Benckiser LLC350764de-7801-b24e-e063-6394a90ab3c32026-05-13WarningsExact identifier
application number: M012
Cepacol Extra Strength Sore Throat and CoughBENZOCAINE AND DEXTROMETHORPHAN HYDROBROMIDEReckitt Benckiser LLCc0cc32db-90f0-4106-8538-89821083ece12026-05-13WarningsExact identifier
application number: M012
Mucinex Cold and FluACETAMINOPHEN, GUAIFENESINReckitt Benckiser LLCe8bc4131-f7b0-926a-e053-2995a90a40ac2026-05-13WarningsExact identifier
application number: M012
Mucinex Cold, Flu, and Sore ThroatACETAMINOPHEN, GUAIFENESINReckitt Benckiser LLC37ded76a-ee8d-f22c-e063-6394a90a00c22026-05-13WarningsExact identifier
application number: M012
Mucinex Night Time Severe Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, AND TRIPROLIDINE HYDROCHLORIDEReckitt Benckiser LLCfdb5c937-c148-eb46-e053-6394a90a8bed2026-05-13WarningsExact identifier
application number: M012
Mucinex Cough Chest CongestionDEXTROMETHORPHAN HBR, GUAIFENESINReckitt Benckiser LLCe9c32d81-cd9b-4ff2-e053-2995a90aa4992026-05-13WarningsExact identifier
application number: M012
Mucinex Nightshift Cold and Flu Maximum StrengthACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND TRIPROLIDINE HYDROCHLORIDEReckitt Benckiser LLC316b5569-b66f-f30c-e063-6394a90ae1472026-05-13WarningsExact identifier
application number: M012
Mucinex Nightshift Cold and Flu Maximum StrengthACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND TRIPROLIDINE HYDROCHLORIDEReckitt Benckiser LLCd9467ca2-df75-4fa1-92b3-d2101eb54a772026-05-13WarningsExact identifier
application number: M012
Mucinex Nightshift Severe Cold and Flu Maximum StrengthACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, AND TRIPROLIDINE HYDROCHLORIDEReckitt Benckiser LLC12420092-3ef6-464b-9106-2d56cd6ef2002026-05-13WarningsExact identifier
application number: M012
Mucinex Nightshift Sinus Maximum StrengthACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, AND TRIPROLIDINE HYDROCHLORIDEReckitt Benckiser LLC09fdf96f-345f-43f2-9f0f-8303ac70849e2026-05-13WarningsExact identifier
application number: M012
Mucinex Childrens Mighty Chews Night Time Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HBR AND DOXYLAMINE SUCCINATEReckitt Benckiser LLC2ce31244-9c6c-b7dd-e063-6394a90a31a82026-05-13WarningsExact identifier
application number: M012
equate daytime cold and fluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDEWal-Mart Stores Inc2ac53cc7-000f-41fd-b799-4e6d6886fe622026-05-13WarningsExact identifier
application number: M012
nighttimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATEPublix Super Markets Inc2201d5c0-bd51-47a7-9775-916b185736232026-05-13WarningsExact identifier
application number: M012
topcare nite time cold and flu reliefACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATETopco Associates LLCf868e4a0-e9fb-4e6a-9984-29a2182462412026-05-13WarningsExact identifier
application number: M012
nitetime cold and fluACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATEMeijer Distribution Inc582fa36b-6d0c-4ff3-80ab-6e0da4b209e42026-05-13WarningsExact identifier
application number: M012
SudoGestPSEUDOEPHEDRINE HYDROCHLORIDEMajor Pharmaceuticals78faa497-6743-b85b-e053-2a91aa0ae8222026-05-12WarningsExact identifier
application number: M012
Allergy Relief mini SoftgelsDIPHENHYDRAMINE HCI 25 MGCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATEDdf1c620b-ff59-4126-99a5-1d6750888f2b2026-05-12WarningsExact identifier
application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1547992camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical GelPSNc6ea663a-9c4f-4d1a-a937-002806a8530a4
1547992camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical GelSCDc6ea663a-9c4f-4d1a-a937-002806a8530a4
1547992camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical GelSYc6ea663a-9c4f-4d1a-a937-002806a8530a4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
52920-133-4852920013348113 g in 1 BOTTLE, PLASTIC (52920-133-48) 113 g2022-11-210000-00-00NoNoCurrent