Label: SUDOGEST- pseudoephedrine hcl tablet, film coated
- NDC Code(s): 0904-5053-24, 0904-5053-59
- Packager: Major Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
If you are a consumer or patient please visit this version.
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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
NDC 0904-5053-59
Compare to the active ingredient
in Sudafed® Sinus Congestion*MAJOR®
Maximum Strength
SudoGest
Pseudoephedrine HCl
30 mg
NASAL DECONGESTANTRelieves:
Sinus Pressure, Sinus CongestionActual Size
100 Tablets
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSINGDistributed by:
MAJOR® PHARMACEUTICALS
Indianapolis, IN 46268
Questions or comments?
Call (800) 616-2471
www.majorpharmaceuticals.com
This product is not manufactured or distributed by
Kenvue Inc., owner of the registered trademark Sudafed®
Sinus Congestion.
50844 REV0619N11212MAJOR 44-112
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INGREDIENTS AND APPEARANCE
SUDOGEST
pseudoephedrine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-5053 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:0904-5053-59 1 in 1 CARTON 08/25/1981 1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:0904-5053-24 1 in 1 CARTON 08/25/1981 11/11/2021 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 Drug M012 08/25/1981 Labeler - Major Pharmaceuticals (191427277) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(0904-5053) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(0904-5053) , pack(0904-5053) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(0904-5053) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(0904-5053) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(0904-5053) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(0904-5053)