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 52 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sinus and Headache DaytimeACETAMINOPHEN, PHENYLEPHRINE HCLDOLGENCORP, LLC869e950c-5861-4840-aaad-b0342790d62b2026-02-10WarningsExact identifier
application number: M012
CareOne Night TIme Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATEAmerican Sales Companyd6b9fb27-3ef7-47ee-81f2-b9a3ccd6de252026-02-10WarningsExact identifier
application number: M012
Medique Cold Cough ProductACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL ,Sportpharm LLCd61df3a4-8ae2-46b1-b322-7f4e04cc1bf92026-02-09WarningsExact identifier
application number: M012
Sinus Congestion and Pain DaytimeACETAMINOPHEN AND PHENYLEPHRINE HCLUnited Natural Foods, Inc. dba UNFIf3fc270a-92fc-46d5-b187-44e875c3abb92026-02-09WarningsExact identifier
application number: M012
Sinus SevereACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCLL.N.K. International, Inc.d5c8b248-6d82-4eac-881c-0b9d0a0de8f12026-02-09WarningsExact identifier
application number: M012
DayTime/NiteTime Severe Cold and Flu Maximum StrengthACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCLMeijer Distribution Incd07112dd-27df-46cc-b7c3-af8ba7601d062026-02-09WarningsExact identifier
application number: M012
TYLENOL Cold Plus Flu Multi-Symptom Liquid Gels Day Plus NightACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE AND DOXYLAMINE SUCCINATEKenvue Brands LLC48f7933e-6582-638c-e063-6394a90abfe52026-02-06WarningsExact identifier
application number: M012
Chest RubCAMPHOR, EUCALYPTUS OIL, MENTHOLRetail Business Services, LLC4fb46860-2bf9-41a7-89eb-31c259c611072026-02-06Warnings, Adverse reactionsExact identifier
application number: M012
pseudoephedrine hydrochloridePSEUDOEPHEDRINE HCLSportpharm LLC909dacfa-50d3-4bcf-b2df-5405427cfaad2026-02-06WarningsExact identifier
application number: M012
Good Sense NasalOXYMETAZOLINE HYDROCHLORIDESportpharm LLCf91b7c1f-e074-4767-b9c8-dbf1937a6a0f2026-02-06WarningsExact identifier
application number: M012
Severe Allergy And Sinus Headache Maximum StrengthACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCLCVS Pharmacyb3c744b8-aa93-505d-f8cf-07995da4283d2026-02-06WarningsExact identifier
application number: M012
NightTime Cold and Flu Multi SymptomACETAMINOPHEN DEXTROMETHORPHAN HYDROBROMIDE DOXYLAMINE SUCCINATEWinCo Foods, LLC911e6a51-c0f0-491a-b70c-00011ed5e35b2026-02-06WarningsExact identifier
application number: M012
Severe Sinus Daytime, Non-DrowsyACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCLWalgreen Companycc0dc951-5024-4517-9d38-a01699407e7e2026-02-06WarningsExact identifier
application number: M012
Chest RubCAMPHOR, EUCALYPTUS OIL, MENTHOLPharmacy Value Alliance, LLCd836c3e2-3b69-41f3-b166-21270550e8ab2026-02-05Warnings, Adverse reactionsExact identifier
application number: M012
Chest RubCAMPHOR, EUCALYPTUS OIL, MENTHOLPublix Super Markets, Inc.81b1d5bb-f813-4f79-9559-2494db33ad3c2026-02-05Warnings, Adverse reactionsExact identifier
application number: M012
NasalOXYMETAZOLINE HYDROCHLORIDEKroger Company6499f854-2995-48cb-9c80-be6524b3db432026-02-05WarningsExact identifier
application number: M012
Cold and Flu plus Congestion DaytimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLWALMART INC.52a398eb-e593-458b-9c42-6f653ca391be2026-02-04WarningsExact identifier
application number: M012
Chest RubCAMPHOR, EUCALYPTUS OIL, MENTHOLHy-Vee, Inc.446de381-6685-748d-e063-6394a90a1b732026-02-04Warnings, Adverse reactionsExact identifier
application number: M012
Severe Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED85aadc86-d979-41a1-849a-e2ccc90144292026-02-04WarningsExact identifier
application number: M012
severe cold and fluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDEHyVee Incfa8c154c-56c6-47de-8e43-9e012b4be95f2026-02-04WarningsExact 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