Pill Identifier Tylenol Cold Max Day - NDC 50580-515
Acetaminophen, Dextromethorphan Hydrobromide, And Phenylephrine Hydrochloride
Product Code 50580-515
Tylenol Cold Max Day by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division is a white oval tablet film coated about 18 mm in size, imprinted with tylenol;1078. The product is a human otc drug with active ingredient(s) acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride.
Tylenol Cold Max Day
Active Ingredient(s): Acetaminophen, Dextromethorphan Hydrobromide, And Phenylephrine Hydrochloride
Inactive Ingredient(s):
- anhydrous citric acid
- carnauba wax
- hypromellose, unspecified
- magnesium stearate
- microcrystalline cellulose
- potassium sorbate
- powdered cellulose
- sodium benzoate
- sodium citrate, unspecified form
- sodium starch glycolate type a potato
- sucralose
Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division
Product Type: Human Otc Drug
Dosage Form: Tablet, Film Coated
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
50580-515-01 | 2 BLISTER PACK in 1 CARTON > 12 TABLET, FILM COATED in 1 BLISTER PACK |
50580-515-02 | 2 BLISTER PACK in 1 CARTON > 12 TABLET, FILM COATED in 1 BLISTER PACK |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.