Twin Med - DIPHENHYDRAMINE HCl Tablets, USP 25mg (55681-322)

Allergy Relief by

Drug Labeling and Warnings

Allergy Relief by is a Otc medication manufactured, distributed, or labeled by TWIN MED LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALLERGY RELIEF- diphenhydramine hydrochloride tablet 
TWIN MED LLC

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Twin Med - DIPHENHYDRAMINE HCl Tablets, USP 25mg (55681-322)

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
• sneezing
• itchy, watery eyes
• itchy nose or throat
• temporarily relieves these symptoms of the common cold:
• runny nose
• sneezing

Warnings

Do not use

• with any other product containing diphenhydramine, even one used on skin
• to make a child sleepy

Ask a doctor before use if you have

• trouble urinating due to an enlarged prostate gland
• glaucoma ? a breathing problem such as emphysema or chronic bronchitis

Ask a doctor or pharmacist before use if youaretaking sedatives or tranquilizers

When using this product

• marked drowsiness may occur
• avoid alcoholic drinks
• excitability may occur, especially in children ? alcohol, sedatives and tranquilizers may increase drowsiness
• be careful when driving a motor vehicle or operating machinery

If pregnant or breast-feeding;

ask a health professional before use

Keep out of reach of children.

In case of accidental overdose, contact a doctor or Poison Control Center immediately. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
Do not exceed recommended dosage.

Directions

• take every 4 to 6 hours, not more than 6 doses in 24 hours
• Adults and children 12 years of age and older:1 or 2 tablets
• children 6 to under 12 years of age:1 tablet
• children 4 to under 6 years of age:do not use unless directed by a doctor
• children under 4 years of age:do not use

Other Information

• each tablet contains : calcium 20 mg
• store at controlled room temperature 20°-25°C (68°-77°F).
• read all product information before using.
• TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

Inactive Ingredients

colloidal silicon dioxide, croscarmellose sodium, dicalcium phosphate, d&c red 27, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, titanium dioxide, talc

Questions or Comments

Questions ? call toll-free 1-844-912-4012

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ITEM# PCOTC124
Distributed by:
ProCure Products
Santa Fe Springs, CA 90670
MADE IN THE U.S.A.

ALLERGY RELIEF 
diphenhydramine hydrochloride tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55681-322
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)
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
POLYVINYL ALCOHOL (UNII: 532B59J990)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	pink	Score	no score
Shape	CAPSULE	Size	11mm
Flavor		Imprint Code	I3
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55681-322-03	300 in 1 BOTTLE; Type 0: Not a Combination Product	07/15/2022	12/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	07/15/2022	12/31/2025

Labeler - TWIN MED LLC (009579330)

Revised: 1/2026

Document Id: 47e2c140-edde-4a38-e063-6294a90a16b8

34390-5

Set id: e4a47131-8017-3d92-e053-2a95a90a619e

Version: 4

Effective Time: 20260108

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