Label: SINUS CONGESTION PE- phenylephrine hcl tablet, film coated
- NDC Code(s): 79903-076-23, 79903-076-24, 79903-076-43
- Packager: WALMART INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 17, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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 79903-076-23
Compare
to SUDAFED
PE® SINUS
CONGESTION
active
ingredient*NON-DROWSY
Sinus Congestion PE
Phenylephrine HCl 10 mg
Nasal DecongestantMAXIMUM STRENGTH
Relieves:
• Sinus Pressure
• Sinus & Nasal CongestionActual Size
10
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 – Or we’ll replace it or give
you your money back. For questions or comments
please call 1-888-287-1915.DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716
PRODUCT OF CHINA, INDIA, AND TAIWAN
*This product is not manufactured or distributed by Johnson & Johnson Corporation,
owner of the registered trademark SUDAFED PE® SINUS CONGESTION.
50844 ORG082045308Equate 44-453
-
INGREDIENTS AND APPEARANCE
SINUS CONGESTION PE
phenylephrine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-076 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DEXTROSE MONOHYDRATE (UNII: LX22YL083G) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) FD&C RED NO. 40 (UNII: WZB9127XOA) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color red Score no score Shape ROUND Size 7mm Flavor Imprint Code 44;453 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-076-24 1 in 1 CARTON 08/31/2021 1 NDC:79903-076-43 24 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:79903-076-23 3 in 1 CARTON 08/31/2021 2 NDC:79903-076-43 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 08/31/2021 Labeler - WALMART INC. (051957769) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(79903-076) , pack(79903-076) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(79903-076) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(79903-076) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(79903-076)