Label: ALLERGY RELIEF PLUS CONGESTION- diphenhydramine hcl, phenylephrine hcl tablet, film coated
- NDC Code(s): 0363-4851-08
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 17, 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:
- runny nose
- sneezing
- nasal congestion
- 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
- difficulty in urination due to enlargement of the prostate gland
- diabetes
- thyroid disease
- heart disease
- glaucoma
- high blood pressure
- a breathing problem such as emphysema or chronic bronchitis
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
NDC 0363-4851-08
Walgreens
Compare to the active ingredients in
Benadryl® Allergy Plus Congestion††WALGREENS PHARMACIST RECOMMENDED†
Allergy Relief
PLUS CONGESTION
DIPHENHYDRAMINE HCl 25 mg / ANTIHISTAMINE
PHENYLEPHRINE HCl 10 mg / NASAL DECONGESTANTCongestion Relief
• Relief of sinus congestion & pressure, runny nose,
sneezing, itchy throat & itchy, watery eyes24
COATED
MINI
TABSACTUAL SIZE
TAMPER EVIDENT: DO
NOT USE IF PACKAGE
IS OPENED OR IF
BLISTER UNIT IS TORN,
BROKEN OR SHOWS
ANY SIGNS OF
TAMPERING†Our pharmacists recommend the Walgreens brand. We invite
you to compare to national brands.
††This product is not manufactured or distributed by Johnson
& Johnson Corporation, owner of the registered trademark
Benadryl® Allergy Plus Congestion.DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com
©2021 Walgreen Co.50844 REV1220A48508
Walgreens 44-485
-
INGREDIENTS AND APPEARANCE
ALLERGY RELIEF PLUS CONGESTION
diphenhydramine hcl, phenylephrine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-4851 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:0363-4851-08 2 in 1 CARTON 11/01/2021 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 11/01/2021 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(0363-4851) , pack(0363-4851) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(0363-4851) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(0363-4851)