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Drug Facts
DIST. BY: PROCTER & GAMBLE, CINCINNATI, OH 45202
The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Vicks (NDC 84126-320). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, active ingredient (per drop), purpose, uses, sore throat warning-, ask a doctor before use if you have, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
DIST. BY: PROCTER & GAMBLE, CINCINNATI, OH 45202
Menthol 20 mg
Oral anesthetic
temporarily relieves occasional minor irritation and pain due to
Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 12 years of age.
ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away
acacia, ascorbyl palmitate, beta carotene, corn syrup, FD&C Blue No. 1, flavor, glycerin, maltodextrin, potassium sorbate, sucrose, sunflower oil, vitamin E DL-alpha, water
1-800-707-1709
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