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 14 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NIGHTTIME SEVERE COLD AND FLUACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCLCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATEDd1115a55-35cd-4f20-8872-f42983a5ebcd2026-07-28WarningsExact identifier
application number: M012
TUSSINDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESINSafewaya5e2bda4-2da6-4c20-855d-2888dadf0c3a2026-07-28WarningsExact identifier
application number: M012
DM MaximumDEXTROMETHORPHAN HBR, GUAIFENESINCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATEDf6029b04-e681-40fc-be4f-14091b76dd4e2026-07-27WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLCVS PHARMACYe958eef1-8aae-4365-ac64-95a9e8e7e0f22026-07-27WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLDOLGENCORP INC38400854-27fa-e291-e063-6294a90a5c4e2026-07-27WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLBetter Living Brands, LLC65802aa7-64e7-4435-ad6b-65895fba17ce2026-07-27WarningsExact identifier
application number: M012
Cold and Flu SevereACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, TRIPROLIDINE HCLWalgreen Company0a48f650-ad2a-4105-9ff4-2bc4d94b46d32026-07-27WarningsExact identifier
application number: M012
Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLWalgreen Company84202ebe-97b6-4be2-bb09-7f2729303f962026-07-27WarningsExact identifier
application number: M012
Daytime Severe Cold and Flu ReliefACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLRite Aid Corporation8d41defe-8120-4cbb-b42e-c805cc5a794b2026-07-24WarningsExact identifier
application number: M012
Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine HydrochlorideACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE AND PHENYLEPHRINE HYDROCHLORIDEProdose, Inc.3afc88c7-388a-dbd9-e063-6294a90a4faf2026-07-24WarningsExact identifier
application number: M012
Giltuss Allergy PlusCHLOPHEDIANOL HCL, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCLGil Pharmaceutical Corp85a0dc7f-ffb5-7d52-e053-2991aa0a602a2026-07-23WarningsExact identifier
application number: M012
Giltuss Cough and ColdDEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLGil Pharmaceutical Corp8590fcc9-c0dd-f43b-e053-2991aa0a692e2026-07-23WarningsExact identifier
application number: M012
Giltuss Sinus and Chest CongestionGUAIFENESIN, PHENYLEPHRINE HCLGil Pharmaceutical Corp8591003c-c2f2-df65-e053-2a91aa0a42fb2026-07-23WarningsExact identifier
application number: M012
COLDTAC PlusACETAMINOPHEN, PHENYLEPHRIN HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDEOPMX LLC3496866c-682f-420b-bfdb-64ecebbf70a22026-07-23WarningsExact identifier
application number: M012
nighttime cough dmDEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATEMeijer, Inc.5a45b4c2-6a15-40b4-9ac6-d1554244ec422026-07-23WarningsExact identifier
application number: M012
DAY TIME NITE TIME INTENSE FLUACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATEMeijer, Inc.6372cbdd-a3a3-499d-91ce-53bcdb83e7392026-07-23WarningsExact identifier
application number: M012
Daytime Nighttime Cold Flu ReliefACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCLCVS Pharmacydf6e522c-3e30-4aa0-8ab9-3b579c80bcad2026-07-22WarningsExact identifier
application number: M012
Cold and Flu NighttimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCLCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED0ab2ba6a-1fac-4a34-ab76-0b50b425d0ba2026-07-22WarningsExact identifier
application number: M012
TYLENOL COLD PLUS FLU MULTI-SYMPTOM GELS NIGHTACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE AND DOXYLAMINE SUCCINATEKenvue Brands LLC1c5386c1-e45d-9dcb-e063-6294a90aff072026-07-22WarningsExact identifier
application number: M012
Allergy plus Sinus HeadacheACETAMINOPHEN 325 MG, DIPHENHYDRAMINE HCL 12.5 MG, PHENYLEPHRINE HCL 5 MGShield Pharmaceuticals Corp772d0184-8c41-40f1-bbef-7e68692eec662026-07-22WarningsExact 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