NDC Code(s) : 70253-453-07, 70253-453-44
Packager : NASH-FINCH COMPANY
Category : HUMAN PRESCRIPTION DRUG LABEL
DEA Schedule : none
Marketing Status : New Drug Application
INGREDIENTS AND APPEARANCE
Suphedrine PEPhenylephrine HCl TABLET, FILM COATED | ||||||||||||||||||||||||||||||
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PRINCIPAL DISPLAY PANEL
SAFETY SEALED
Relieves Nasal and
Sinus Congestion Due
to Colds and Allergies
Our Family®
Quality Care Since 1904
Compare to the Active ingredient of Sudafed PE®*
Suphedrine PE
PHENYLEPHRINE HYDROCHLORIDE
NASAL DECONGESTANT
WITHOUT DROWSINESS
18 TABLETS
Does not contain Pseudoephedrine
1 Pill Per Dose
10 mg EACH
TAMPER EVIDENT: DO NOT USE IF CATON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
*This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Sudafed PE®.
50844 REV1111E45344
DISTRIBUTED BY:
NASH FINCH COMPANY ©2004, 1996
NFC BRANDS
7600 FRANCE AVE S, MPLS, MN 55435
www.ourfamilyfoods.com NF16559