FDA.reportPublic FDA data

cough suppressant and topical analgesic

Product NDC
11673-667
11-digit product format
116730667
Labeler code
11673
Product ID
11673-667_4b1e7206-1f3d-b750-e063-6394a90a36dc
Type
HUMAN OTC DRUG
Nonproprietary name
Camphor, Eucalyptus oil, Menthol
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Target Corporation
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2009-01-27
Substance
CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL
Active strength
48; 12; 26 mg/g; mg/g; mg/g
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
cough suppressant and topical analgesic
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAMPHOR (SYNTHETIC)48 mg/g
EUCALYPTUS OIL12 mg/g
MENTHOL26 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

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

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
727137Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
df21d9d6-36a9-49cf-a29c-c4a573899bd5Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-667-02cough suppressant and topical analgesic1 in 1 CARTONOINTMENT117
11673-667-02cough suppressant and topical analgesic49.8 g in 1 JAROINTMENT49.817

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ETUP AND UP COUGH SUPPRESSANT AND TOPICAL ANALGESIC CHEST RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL NATURAL) OINTMENT [TARGET CORPORATION]3
EUCALYPTUS OILACTIVE INGREDIENT2R04ONI662UP AND UP COUGH SUPPRESSANT AND TOPICAL ANALGESIC CHEST RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL NATURAL) OINTMENT [TARGET CORPORATION]3
MENTHOLACTIVE INGREDIENTL7T10EIP3AUP AND UP COUGH SUPPRESSANT AND TOPICAL ANALGESIC CHEST RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL NATURAL) OINTMENT [TARGET CORPORATION]3
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ETUP AND UP COUGH SUPPRESSANT AND TOPICAL ANALGESIC CHEST RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL NATURAL) OINTMENT [TARGET CORPORATION]3
EUCALYPTUS OILACTIVE MOIETY2R04ONI662UP AND UP COUGH SUPPRESSANT AND TOPICAL ANALGESIC CHEST RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL NATURAL) OINTMENT [TARGET CORPORATION]3
MENTHOLACTIVE MOIETYL7T10EIP3AUP AND UP COUGH SUPPRESSANT AND TOPICAL ANALGESIC CHEST RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL NATURAL) OINTMENT [TARGET CORPORATION]3
PETROLATUMINACTIVE INGREDIENT4T6H12BN9UUP AND UP COUGH SUPPRESSANT AND TOPICAL ANALGESIC CHEST RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL NATURAL) OINTMENT [TARGET CORPORATION]3
THYMOLINACTIVE INGREDIENT3J50XA376EUP AND UP COUGH SUPPRESSANT AND TOPICAL ANALGESIC CHEST RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL NATURAL) OINTMENT [TARGET CORPORATION]3
TURPENTINEINACTIVE INGREDIENTXJ6RUH0O4GUP AND UP COUGH SUPPRESSANT AND TOPICAL ANALGESIC CHEST RUB (CAMPHOR, EUCALYPTUS OIL, MENTHOL NATURAL) OINTMENT [TARGET CORPORATION]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-667COUGH SUPPRESSANT AND TOPICAL ANALGESIC (CAMPHOR, EUCALYPTUS OIL, MENTHOL) OINTMENT [TARGET CORPORATION]16Current NDC, Legacy NDC, 2 package rows20250322_df21d9d6-36a9-49cf-a29c-c4a573899bd5.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 35 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Allergy Childrens AllergyDIPHENHYDRAMINE HYDROCHLORIDEDolgencorp, Inc. (DOLLAR GENERAL & REXALL)047102c4-3d03-4b2d-961d-0ac75980147b2026-05-06WarningsExact identifier
application number: M012
GOOD SENSE COMBO PACK DAYTIME AND NIGHTTIMEACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDEL. Perrigo Companyd25f2649-4f8a-4339-8443-faa0b98bdd702026-05-06WarningsExact identifier
application number: M012
Allergy Relief 4 HourCHLORPHENIRAMINE MALEATEWinCo Foods, LLC27e911e1-6d22-4a50-8413-1809c8973cbd2026-05-06WarningsExact identifier
application number: M012
ALKA SELTZER COLD Cold Cough Maximum Strength Fast GelsACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDEBayer HealthCare LLC.51173330-d537-fb9c-e063-6394a90ae3422026-05-05WarningsExact identifier
application number: M012
Equate daytime severe vaporice cold and flu nighttime severe vapor ice cold and fluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATEWal-Mart Stores Inc08e74a8d-8e8d-4cda-9adc-ea2ff40683532026-05-05WarningsExact identifier
application number: M012
GOODSENSE COMBO PACK DAYTIME AND NIGHTTIMEACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HCLL. Perrigo Companye42f9e0d-f990-4c33-af43-75acf5d776382026-05-05WarningsExact identifier
application number: M012
Rugby Mucus and Chest Congestion 541GUAIFENESINRugby Laboratories76472912-b66f-4bb4-937a-4a589683a78c2026-05-04WarningsExact identifier
application number: M012
Sinus Congestion and Pain Daytime Non-DrowsyACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDEH E Be9dd2d7b-0a19-4a42-b51e-b9914f02406e2026-05-04WarningsExact identifier
application number: M012
Sanatos NighttimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATEPharmadel LLC3dd3ed85-0c0a-8390-e063-6294a90a668e2026-05-04WarningsExact identifier
application number: M012
Good Sense Daytime non drowsy cold and fluACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLL. Perrigo Company0122cd34-5817-4af5-a51a-8d176dee0a302026-05-04WarningsExact identifier
application number: M012
COLD AND FLU RELIEFACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLSafewayd810a6a9-6112-4e9d-a396-36084b7e110e2026-05-04WarningsExact identifier
application number: M012
Benadryl Allergy UltratabDIPHENHYDRAMINE HYDROCHLORIDESavings Distributors LLC8d59d121-62a8-c43b-e053-2a95a90a58472026-05-01WarningsExact identifier
application number: M012
Tylenol Cold Plus Flu SevereACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDESavings Distributors LLC8e87f8de-f83e-0f8d-e053-2a95a90a8d6a2026-05-01WarningsExact identifier
application number: M012
Tylenol Sinus SevereACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDESavings Distributors LLC8eecb3f0-eb5e-e847-e053-2995a90a86bd2026-05-01WarningsExact identifier
application number: M012
Sinus Pressure and Congestion Relief PE Maximum StrengthPHENYLEPHRINE HCLRite Aid Corporationfccea3c5-42af-4939-82bc-d9409b75f91f2026-05-01WarningsExact identifier
application number: M012
Night Time Cold and Flu originalACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATEHarris Teeter, LLCcfaf4b3d-fab4-424d-adbe-aaedca58912d2026-04-30WarningsExact identifier
application number: M012
Nighttime Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATEHarris Teeter, LLC21e7d323-5b78-43aa-b0fc-34c2a864ab9a2026-04-30WarningsExact identifier
application number: M012
daytime severe cold and fluACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLH E Bec0b5f4b-b58c-445f-acf1-c7ce301bba642026-04-30WarningsExact identifier
application number: M012
Mucus Relief DM Max Maximum StrengthDEXTROMETHORPHAN HBR, GUAIFENESINHarris Teeter, LLC098428ae-e87d-4c29-8f02-1590530da58e2026-04-29WarningsExact identifier
application number: M012
Panadol Cold and Flu DayACETAMINOPHEN, DEXTROMETHORPHAN HBRHaleon US Holdings LLC341761b9-f0be-f816-e063-6394a90a5e632026-04-29WarningsExact identifier
application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical OintmentPSNdf21d9d6-36a9-49cf-a29c-c4a573899bd517
727137camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical OintmentSCDdf21d9d6-36a9-49cf-a29c-c4a573899bd517
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Chest RubSYdf21d9d6-36a9-49cf-a29c-c4a573899bd517
727137camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical OintmentSYdf21d9d6-36a9-49cf-a29c-c4a573899bd517

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-667-02116730667021 JAR in 1 CARTON (11673-667-02) / 49.8 g in 1 JAR1 jar2009-01-270000-00-00NoNoCurrent