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
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated February 13, 2023
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- Active Ingredients
- 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.
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
- adverse reactions section
- Principal display panel
INGREDIENTS AND APPEARANCE
COUGH SUPPRESSANT AND TOPICAL ANALGESIC
camphor, eucalyptus oil, menthol ointment
Product 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 final part341 01/27/2009 Labeler - Target Corporation (006961700) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(11673-667) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(11673-667)