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 93 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VANACOF DMDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDEGM Pharmaceuticals, INC2ed699f2-d004-4fa9-8042-6c85a9ff69b62025-11-03WarningsExact identifier
application number: M012
Geri DrylDIPHENHYDRAMINE HCLVERITYRX, LLC42a05f69-0599-5571-e063-6394a90a37d32025-11-02WarningsExact identifier
application number: M012
M-DrylDIPHENHYDRAMINE HYDROCHLORIDEVERITYRX, LLC42a0e577-a1b6-2c16-e063-6294a90af8e32025-11-02WarningsExact identifier
application number: M012
Severe Sinus Congestion and PainACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINEShield Pharmaceuticals Corpc296efd0-5030-4a26-a9b0-e66423d995dc2025-10-31WarningsExact identifier
application number: M012
Daytime Cold and Flu Max Maximum Strength SoftgelsACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLTopco Associates, LLCf7ebe482-cb22-4517-8463-3432cf60071d2025-10-31WarningsExact identifier
application number: M012
Nighttime Cold and Flu Max SoftgelsACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCLTopco Associates, LLC787bff76-0ee2-4e7e-b908-876e4a3e3bfc2025-10-31WarningsExact identifier
application number: M012
Honey Lemon Cough DropsMENTHOLTrader Joe's Company647dadae-f37a-8399-e053-2991aa0aedb32025-10-31WarningsExact identifier
application number: M012
Family Care SalineSODIUM CHLORIDEUnited Exchange Corp.06737393-d4ae-3e7b-e063-6394a90ac19f2025-10-31WarningsExact identifier
application number: M012
QUALITY CHOICE Maximum Strength Daytime Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDEChain Drug Marketing Association, Inc.40416ff5-06e1-97dd-e063-6394a90a20462025-10-30WarningsExact identifier
application number: M012
Robitussin Maximum Strength Nighttime Cough DMDEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATEHaleon US Holdings LLC44feee2f-25bc-48d4-8e13-db1d9daaaa902025-10-30WarningsExact identifier
application number: M012
Robitussin Day and Night Cough Relief DM MaxDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, DOXYLAMINE SUCCINATEHaleon US Holdings LLCb3d02c91-8f79-4eb4-a378-1072474c572c2025-10-30WarningsExact identifier
application number: M012
ROBITUSSIN MAXIMUM STRENGTH COUGH PLUS CHEST CONGESTION DMDEXTROMETHORPHAN HBR, GUAIFENESINHaleon US Holdings LLCf1d022dd-c2ca-497f-87d5-9ef3e20e8ea72025-10-30WarningsExact identifier
application number: M012
EndalTRIPROLIDINE HCL, DEXTROMETHORPHAN HBRPoly Pharmaceuticals, Inc.fc5401e2-ed65-72e7-e053-6294a90a81f32025-10-30WarningsExact identifier
application number: M012
daytimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLPublix Super Markets Incc7cef266-46fc-49ab-a2e7-54fc562986592025-10-30WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HYDROCHLORIDESAM'S WEST INC16592ad7-b7cb-0837-e063-6394a90ae0592025-10-29WarningsExact identifier
application number: M012
Maximum Strength Severe Congestion and CoughDEXTROMETHORPHAN HBR, GUAIFENESIN, AND PHENYLEPHRINE HCLSAFEWAY013b94a1-26c7-4371-981a-d1b9d7fd1c982025-10-29WarningsExact identifier
application number: M012
Better LivingPHENYLEPHRINE HYDROCHLORIDEBETTER LIVING BRANDS LLCaea0db7f-e01a-4d8e-9c20-4a5ef4a905d12025-10-29WarningsExact identifier
application number: M012
AXIM DayTime - Night Time 72 SoftgelsACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDEVIVUNT PHARMA LLCde9eb2d5-ba51-4637-e053-2995a90a04512025-10-29WarningsExact identifier
application number: M012
Dollar General Vapor SteamCAMPHOR (SYNTHETIC)DOLGENCORP, LLC86d0f3ac-1359-c2f9-e053-2a91aa0a35d02025-10-29WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLStrategic Sourcing Services LLC5d628b09-c257-4369-8ddb-47554d83c0d82025-10-29WarningsExact 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