NDC | 59779-953-07, 59779-953-23 |
Set ID | ac7ee445-f430-4189-82ff-add6e8f65aea |
Category | HUMAN OTC DRUG LABEL |
Packager | CVS Pharmacy |
Generic Name | |
Product Class | alpha-1 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
- 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
♥︎CVS Health™
Compare to the active ingredient in Sudafed PE® Congestion*
NDC 59779-953-23
Non-Drowsy
Sinus PE Decongestant
PHENYLEPHRINE HYDROCHLORIDE
Nasal decongestantMAXIMUM STRENGTH
Relieves
• Sinus pressure
• Nasal congestion72 TABLETS
Actual Size
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 McNeil Consumer Healthcare, owner of the registered trademark Sudafed PE® Congestion.
50844 REV0715A45323Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2015 CVS/pharmacy
CVS.com® 1-800-SHOP CVSV-19849
√ CVS® Quality
Money Back GuaranteeCVS Health 44-453
-
INGREDIENTS AND APPEARANCE
SINUS PE DECONGESTANT MAXIMUM STRENGTH
phenylephrine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-953 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) FD&C RED NO. 40 (UNII: WZB9127XOA) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) 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:59779-953-23 3 in 1 CARTON 01/14/2005 04/24/2022 1 24 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:59779-953-07 2 in 1 CARTON 01/14/2005 04/24/2022 2 18 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 01/14/2005 04/24/2022 Labeler - CVS Pharmacy (062312574) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(59779-953) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 pack(59779-953) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(59779-953) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 pack(59779-953) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(59779-953)