Label: COUGH SUPPRESSANT AND TOPICAL ANALGESIC- camphor, eucalyptus oil, menthol ointment
- NDC Code(s): 11673-667-02
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 25, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before us if you have
- When using this product, do not
- Stop use and ask a doctor if
- If pregnant or breast-feeding
- Keep out of reach of children.
-
Directions
see important warnings under "When using this product"
- adults & children 2 yrs & over:
- rub a thick layer on chest and throat or rub on sore aching muscles
- cover with a warm dry cloth if desired
- keep clothing loose about thorat/chest to help vapors reach the nose/mouth
- repeat up to three times per 24 hours or directed by doctor
- children under 2 years of age: ask a doctor
- Other information
- Inactive ingredients
- Questions?
- adverse reactions section
- Principal display panel
-
INGREDIENTS AND APPEARANCE
COUGH SUPPRESSANT AND TOPICAL ANALGESIC
camphor, eucalyptus oil, menthol ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-667 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 48 mg in 1 g EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL 12 mg in 1 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 26 mg in 1 g Inactive Ingredients Ingredient Name Strength CEDAR LEAF OIL (UNII: BJ169U4NLG) NUTMEG OIL (UNII: Z1CLM48948) PETROLATUM (UNII: 4T6H12BN9U) TURPENTINE (UNII: XJ6RUH0O4G) THYMOL (UNII: 3J50XA376E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-667-02 1 in 1 CARTON 01/27/2009 1 49.8 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 01/27/2009 Labeler - Target Corporation (006961700) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(11673-667)