Label: ALLERGY RELIEF- diphenhydramine hydrochloride tablet, film coated
- NDC Code(s): 79903-272-10, 79903-272-20
- Packager: Walmart Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 8, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (in each tablet) Diphenhydramine HCl 25 mg
- Purpose Antihistamine
- Uses ■ temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: ■ runny nose ■ itchy, watery eyes ■ sneezing ■ itching of the nose or throat ■ temporarily relieves these symptoms due to the common cold: ■ runny nose ■ sneezing
- Warnings
- Do not use■ to make a child sleepy ■ with any other product containing diphenhydramine, even one used on skin
- Ask a doctor before use if you have ■ a breathing problem such as emphysema or chronic bronchitis ■ trouble urinating due to an enlarged prostate gland ■ glaucoma
- Ask a doctor or pharmacist before useif you are taking sedatives or tranquilizers
- When using this product ■ marked drowsiness may occur ■ avoid alcoholic drinks ■ alcohol, sedatives and tranquilizers may increase drowsiness ■ be careful when driving a motor vehicle or operating machinery ■ excitability may occur, especially in children
- If pregnant or breast-feeding,ask a health professional before use.
- Keep out of reach of children.In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
- Directions ■ take every 4 to 6 hours, or as directed by a doctor ■ do not take more than 6 times in 24 hours adults and children 12 years and over 1 to 2 tablets children 6 to under 12 years 1 tablet children under 6 years do not use
- Other information ■ each tablet contains:calcium 25 mg ■ store between 20-25° C (68-77° F) ■ protect from moisture and light
- Inactive ingredients colloidal silicon dioxide, croscarmellose sodium, dicalcium phosphate, D&C red # 27 aluminum lake, lecithin, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, talc, titanium dioxide
- Questions or comments?1-888-287-1915
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
diphenhydramine hydrochloride tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-272 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 Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) D&C RED NO. 27 (UNII: 2LRS185U6K) ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color pink Score no score Shape CAPSULE Size 12mm Flavor Imprint Code S4 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-272-20 2 in 1 CARTON 05/08/2024 1 NDC:79903-272-10 100 in 1 BOTTLE; 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 05/08/2024 Labeler - Walmart Inc. (051957769)
