Label: ALLERGY PLUS SINUS RELIEF- diphenhydramine hcl and phenylephrine hcl tablet, film coated
- NDC Code(s): 11822-0485-8
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients (in each tablet)
- Purpose
-
Uses
- temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- nasal congestion
- runny nose
- sneezing
- itching of the nose or throat
- itchy, watery eyes
- temporarily relieves these symptoms due to the common cold:
- nasal congestion
- runny nose
- sneezing
- temporarily relieves sinus congestion and pressure
- temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
-
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.
- with any other product containing diphenhydramine, even one used on skin
Ask a doctor before use if you have
- heart disease
- diabetes
- high blood pressure
- difficulty in urination due to enlargement of the prostate gland
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- thyroid disease
When using this product
- do not exceed recommended dosage
- excitability may occur, especially in children
- marked drowsiness may occur
- alcohol, sedatives, and tranquilizers may increase drowsiness
- avoid alcoholic beverages
- use caution when driving a motor vehicle or operating machinery
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal display panel
Compare to the active ingredients in
Benadryl® Allergy Plus Congestion*ALLERGY PLUS
SINUS RELIEF
PHENYLEPHRINE HCl
DIPHENHYDRAMINE HClANTIHISTAMINE
NASAL DECONGESTANT
RELIEF OF
Sneezing, runny nose, sinus congestion,
sinus pressure, itchy throat,
& itchy, watery eyes24
TABLETS*This product is not manufactured or distributed by Johnson & Johnson
Corporation, owner of the registered trademark Benadryl® Allergy Plus Congestion.
50844 ORG122048508DISTRIBUTED BY:
RITE AID, 200 NEWBERRY COMMONS,
ETTERS, PA 17319 www.riteaid.comSATISFACTION GUARANETT: If you're not
satisfied, we'll happily refund your money.TAMPER EVIDENT: DO NOT USE IF PACKAGE IS
OPENED OR IF BLISTER UNIT IS TORN, BROKEN
OR SHOWS ANY SIGNS OF TAMPERINGRite Aid 44-485
-
INGREDIENTS AND APPEARANCE
ALLERGY PLUS SINUS RELIEF
diphenhydramine hcl and phenylephrine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0485 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYDEXTROSE (UNII: VH2XOU12IE) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIACETIN (UNII: XHX3C3X673) Product Characteristics Color blue Score no score Shape OVAL Size 11mm Flavor Imprint Code 44;485 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0485-8 2 in 1 CARTON 08/10/2005 1 12 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 08/10/2005 Labeler - Rite Aid Corporation (014578892) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(11822-0485) , pack(11822-0485) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(11822-0485) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(11822-0485)