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 23 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Theraflu Severe Congestion Relief Cooling Nasal MistOXYMETAZOLINE HCLHaleon US Holdings LLC90125a19-eed7-4ca4-a6dc-f38026c74d542026-06-08WarningsExact identifier
application number: M012
Severe Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLWalgreen Company54254b61-7861-4eeb-bd3c-54fd5266f4a72026-06-08WarningsExact identifier
application number: M012
GuaifenesinGUAIFENESINMajor Pharmaceuticalsaa662428-e61f-4e22-af4d-8cf63df68c992026-06-08WarningsExact identifier
application number: M012
Daytime NighttimeACETAMINOPHEN, GUAIFENESIN AND ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCLTARGET CORPORATION47a218a0-6395-36bd-e063-6394a90a265a2026-06-05WarningsExact identifier
application number: M012
Daytime NighttimeACETAMINOPHEN DEXTROMETHORPHAN HBR, ACETAMINOPHEN DEXTROMETHORPHAN HBR TRIPROLIDINE HCLTARGET CORPORATION4779288a-9850-8490-e063-6394a90abe512026-06-05WarningsExact identifier
application number: M012
Mucinex Fast-Max DM Max and Mucinex Fast-Max Nighttime DM Max Value PackDEXTROMETHORPHAN HBR, GUAIFENESIN AND TRIPROLIDINE HCLReckitt Benckiser LLC4df37cfb-299f-661f-e063-6394a90ab3372026-06-04WarningsExact identifier
application number: M012
ALKA SELTZER COLD Cold Flu Congestion Severe Fast Hot Liquid Day NightACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, AND DOXYLAMINE SUCCINATEBayer HealthCare LLC.53715ea4-42b3-5887-e063-6294a90a42492026-06-04WarningsExact identifier
application number: M012
Tussin DMDEXTROMETHORPHAN HBR, GUAIFENESINChain Drug Marketing Association, Inc.b0d38db9-22a9-4dd8-8e0f-dd81805e724b2026-06-04WarningsExact identifier
application number: M012
Cough and Cold HBPCHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBRCVS PHARMACY65d4d7ea-c080-404e-9836-7d6bdcc5ea7d2026-06-04WarningsExact identifier
application number: M012
Allergy Relief ChildrensDIPHENHYDRAMINE HCLCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATEDfe9d6a6e-38a1-44ae-a30f-596c5ec7d0572026-06-03WarningsExact identifier
application number: M012
Severe Congestion and CoughDEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLWalgreen Companyb0c1d635-0f85-433a-b479-51c68d259faa2026-06-03WarningsExact identifier
application number: M012
Cold and Flu NighttimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCLWalgreen Companyde4e8af4-d3d0-44b3-aea3-79016803ccdc2026-06-03WarningsExact identifier
application number: M012
Mucus Relief DMDEXTROMETHORPHAN HBR AND GUAIFENESINARMY AND AIR FORCE EXCHANGE SERVICEdc0a3761-bbe2-4261-a183-594f5fb12b0b2026-06-03WarningsExact identifier
application number: M012
Cold and Flu Daytime, NighttimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCLWALMART INC.f278cc81-65b2-4e45-be5b-41152cbb67c42026-06-03WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLFamily Dollar Services Inc358ba91d-06a4-49c9-994d-4e4bf9499dcd2026-06-03WarningsExact identifier
application number: M012
GUAIFENESIN DMGUAIFENESIN AND DEXTROMETHORPHANCardinal Health 107, LLCc5fd53c9-81d6-4ce6-88a0-c2c24e17a7ed2026-06-02WarningsExact identifier
application number: M012
ALKA SELTZER COLD Cold and Flu plus Congestion Severe Fast Hot Liquid NightACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND PHENYLEPHRINE HYDROCHLORIDEBayer HealthCare LLC.5349dbde-730c-610f-e063-6394a90a952a2026-06-02WarningsExact identifier
application number: M012
Guaifenesin and Codeine PhosphateGUAIFENESIN AND CODEINE PHOSPHATECardinal Health 107, LLCa9130f36-4761-4e6b-a383-eca3db06ea932026-06-02WarningsExact identifier
application number: M012
Topcare Day Time Nite Time Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HCLTopco Associates LLCaed387e0-5a8b-4caf-a373-3e04496a49832026-06-02WarningsExact identifier
application number: M012
ALKA SELTZER COLD Cold Flu And Congestion Severe Fast Hot Liquid DayACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDEBayer HealthCare LLC.53371691-2510-5039-e063-6394a90a6ea92026-06-01WarningsExact 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