Pill Identifier Sudafed Pe Pressure Plus Pain - NDC 50580-547
Acetaminophen And Phenylephrine Hydrochloride
Product Code 50580-547
Sudafed Pe Pressure Plus Pain by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division is a orange oval tablet film coated about 18 mm in size, imprinted with su;pe;wl;89. The product is a human otc drug with active ingredient(s) acetaminophen and phenylephrine hydrochloride.
Sudafed Pe Pressure Plus Pain
Active Ingredient(s): Acetaminophen And Phenylephrine Hydrochloride
Inactive Ingredient(s):
- carnauba wax
- FD&C Yellow no. 6
- aluminum oxide
- hypromellose, unspecified
- magnesium stearate
- microcrystalline cellulose
- polyethylene glycol, unspecified
- polysorbate 80
- powdered cellulose
- sodium starch glycolate type a potato
- titanium dioxide
Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division
Product Type: Human Otc Drug
Dosage Form: Tablet, Film Coated
- Orange (C48331)
Product Packages
NDC Package Code | Package Description |
---|---|
50580-547-25 | 2 BLISTER PACK in 1 CARTON > 12 TABLET, FILM COATED in 1 BLISTER PACK |
50580-547-73 | 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.