ADULT ALLERGY RELIEF DYE FREE- diphenhydramine hydrochloride solution

Adult Allergy Relief by

Drug Labeling and Warnings

Adult Allergy Relief by is a Otc medication manufactured, distributed, or labeled by WALGREEN COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient [in each 10 mL]

Diphenhydramine HCl, USP 25 mg

Purpose

Antihistamine

Uses

• ▪ temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
  • ▪ sneezing
  • ▪ itchy, watery eyes
  • ▪ runny nose
  • ▪ itching of the nose or throat

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 chronic bronchitis
• ▪ glaucoma
• ▪ a sodium-restricted diet
• ▪ trouble urinating due to enlarged prostate

Ask a doctor or pharmacist before use if 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

• ▪ measure only with dosing cup provided
• ▪ Keep dosing cup with product
• ▪ mL = milliliter
• ▪ do not take more than 6 doses in 24 hours

• Age (yr):

  Dose (mL) ;

• Adult and children 12 years and older:

  10 mL to 20 mL (2 to 4 tsp) every 4 to 6 hrs;

• Children under 12 years:

  Do not use;

Other information

• each 10 mL contains: sodium 30 mg
• store at room temperature. Store in outer carton until contents used
• do not refrigerate
• see bottom panel for lot number and expiration date
• protect from light
• ask a doctor before use if you have a sodium restricted diet.

Inactive ingredients

anhydrous citric acid, carboxymethylcellulose sodium, flavors, glycerin, potassium citrate, purified water, sodium benzoate, sorbitol, sucralose

Questions or Comments?

1-866-467-2748

Package Label-Principal Display Panel 4 Fl Oz (118 Ml Bottle)

NDC: 0363-7100-04

Dye-Free

AdultAllergyRelief

Diphenhydramine HCl | Antihistamine

For Relief of:

• Runny nose
• Itchy, watery eyes
• Sneezing and Itchy Watery Eyes

Sugar Free
Cherry Flavor

Naturally and Artificially Flavored

4 FL OZ (118 mL)

IMPORTANT: Keep this carton for future reference on full labeling.

INGREDIENTS AND APPEARANCE

ADULT ALLERGY RELIEF  DYE FREE
diphenhydramine hydrochloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-7100
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  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
CHERRY (UNII: BUC5I9595W)
GLYCERIN (UNII: PDC6A3C0OX)
POTASSIUM CITRATE (UNII: EE90ONI6FF)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITOL (UNII: 506T60A25R)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	YELLOW (Colorless to Pale Yellow)	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-7100-04	1 in 1 CARTON	01/30/2020
1		118 mL 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 final	part341	01/30/2020

Labeler - WALGREEN COMPANY (008965063)