Label: SINUS CONGESTION- phenylephrine hcl tablet, film coated
- NDC Code(s): 30142-853-07, 30142-853-23
- Packager: Kroger Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 12, 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
Kroger®
COMPARE TO the active ingredient of SUDAFED PE® CONGESTION *See bottom panel
NDC 30142-853-07
Maximum Strength
Sinus Congestion
Phenylephrine HCl 10 mg
Nasal DecongestantNON-DROWSY
RELIEVES:
• Sinus Pressure
• Nasal & Sinus Congestionactual size
36 TABLETS
Our Pharmacists Recommended
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERINGOur Brands. Our Guarantee.
Love it or Your Money Back.
www.kroger.comDISTRIBUTED BY THE KROGER CO.
CINCINNATI, OHIO 45202FOR MORE PRODUCT INFORMATION, SCAN UPC
USING YOUR KROGER APP OR CALL 800-632-6900*Sudafed PE® Sinus Congestion is a registered trademark of Johnson
& Johnson Corporation, New Brunswick, NJ 08933. Johnson & Johnson
Corporation is not affiliated with the Kroger Co. or this product.
50844 ORG082045307
Kroger 44-453
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INGREDIENTS AND APPEARANCE
SINUS CONGESTION
phenylephrine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-853 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:30142-853-07 2 in 1 CARTON 03/19/2021 1 18 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:30142-853-23 3 in 1 CARTON 03/19/2021 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 03/19/2021 Labeler - Kroger Company (006999528) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(30142-853) , pack(30142-853) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(30142-853) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(30142-853) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(30142-853)