Label: SINUS AND CONGESTION NON-DROWSY- pseudoephedrine hcl tablet, film coated
- NDC Code(s): 49035-780-08, 49035-780-22, 49035-780-43
- Packager: Wal-Mart Stores Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 7, 2024
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- Official Label (Printer Friendly)
- 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
- heart disease
- diabetes
- thyroid disease
- high blood pressure
- difficulty in urination due to enlargement of the prostate gland
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
equate™
NDC 49035-780-08
Compare to Sudafed®
Sinus Congestion
active ingredient*NON-DROWSY
Sinus & Congestion
Pseudoephedrine HCl 30 mg
Nasal DecongestantMAXIMUM STRENGTH
Relief of:
• Sinus congestion • Sinus pressureActual Size
30
mg EACH24
TABLETSTAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERINGSatisfaction guaranteed - For questions or
comments please call 1-888-287-1915.DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716
PRODUCT OF CHINA, GERMANY, AND INDIA
*This product is not manufactured or distributed by
Johnson & Johnson Corporation, owner of the registered
trademark Sudafed® Sinus Congestion.
50844 ORG061911208Equate 44-112
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INGREDIENTS AND APPEARANCE
SINUS AND CONGESTION NON-DROWSY
pseudoephedrine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-780 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 ALUMINUM LAKE (UNII: GYP6Z2JR6Q) 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:49035-780-43 24 in 1 BLISTER PACK; Type 0: Not a Combination Product 07/15/2020 2 NDC:49035-780-08 1 in 1 CARTON 07/15/2020 2 24 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:49035-780-22 2 in 1 CARTON 07/15/2020 3 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 Drug M012 07/15/2020 Labeler - Wal-Mart Stores Inc (051957769) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(49035-780) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(49035-780) , pack(49035-780) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(49035-780) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(49035-780) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(49035-780) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(49035-780)