NDC | 11822-0112-2, 11822-0112-8 |
Set ID | d86140ab-1117-4d14-a380-f5cc375775a1 |
Category | HUMAN OTC DRUG LABEL |
Packager | Rite Aid Corporation |
Generic Name | |
Product Class | alpha-Adrenergic Agonist |
Product Number | |
Application Number | PART341 |
- Active ingredient (in each tablet)
- Purpose
- Uses
-
Warnings
Do not use
if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
Ask a doctor before use if you have
- diabetes
- heart disease
- high blood pressure
- thyroid disease
- difficulty in urination due to enlargement of the prostate gland
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
Compare to the active ingredient in Sudafed® Sinus Congestion*
MAXIMUM STRENGTH
Sinus Pressure &
Congestion ReliefPseudoephedrine HCl 30 mg
nasal decongestant
Relieves: sinus pressure, nasal and sinus congestion
NON-DROWSY
ACTUAL SIZE
24 TABLETS
TAMPER EVIDENT: DO NOT USE IF
PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS
ANY SIGNS OF TAMPERING*This product is not manufactured or distributed by
Johnson & Johnson Corporation, owner of the
registered trademark Sudafed® Sinus Congestion.
50844 REV0619C11208DISTRIBUTED BY:
RITE AID, 30 HUNTER LANE
CAMP HILL, PA 17011
www.riteaid.comSATISFACTION
GUARANTEE
If you're not satisfied, we'll
happily refund your moneyRite Aid 44-112
-
INGREDIENTS AND APPEARANCE
SINUS PRESSURE AND CONGESTION RELIEF MAXIMUM STRENGTH
pseudoephedrine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0112 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE 30 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYDEXTROSE (UNII: VH2XOU12IE) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIACETIN (UNII: XHX3C3X673) Product Characteristics Color red Score no score Shape ROUND Size 7mm Flavor Imprint Code 44;112 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0112-8 1 in 1 CARTON 08/25/1981 1 24 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:11822-0112-2 2 in 1 CARTON 08/25/1981 2 24 in 1 BLISTER PACK; 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 08/25/1981 Labeler - Rite Aid Corporation (014578892) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(11822-0112) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(11822-0112) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 pack(11822-0112) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 pack(11822-0112) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(11822-0112)