ALLERGY- diphenhydramine hydrochloride capsule

Allergy by

Drug Labeling and Warnings

Allergy by is a Otc medication manufactured, distributed, or labeled by Mckesson. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

(per capsule)

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms of hay fever or other upper respiratory allergies:

• runny nose
• itching of the nose or throat
• sneezing
• itchy, watery eyes

  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
• glaucoma
• trouble urinating due to an enlarged prostate gland

  Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

  When using this product

• you may get very drowsy
• avoid alcoholic drinks
• alcohol, sedatives & 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 right away. (1-800-222-1222)

Directions

• take every 4 to 6 hours
• do not take more than 6 tablets in 24 hours
  • Age (Yr): Dose (capsules)
  • Adults and children 12 years of age and over: Take 1 to 2 capsules
  • Children 6 to under 12 years of age: Take 1 capsule
  • Children under 6 years of age: do not use

Other Information

• store at room temperature between 15°-30°C (59°-86°F)
• protect from light and moisture

Inactive Ingredients

Benzyl alcohol, Butyl paraben, D&C red # 28, FD&C blue # 1, FD&C  red # 40, Edible black ink, gelatin, lactose, Magnesium stearate, Methyl paraben, polysorbate 80, Propyl paraben, Purified water, Sodium lauryl sulfate, Starch

Questions or Comments

Call 1-855-314-1850

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 70677-0010-1

INGREDIENTS AND APPEARANCE

ALLERGY 
diphenhydramine hydrochloride capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70677-0010
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
BENZYL ALCOHOL (UNII: LKG8494WBH)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
D&C RED NO. 28 (UNII: 767IP0Y5NH)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GELATIN (UNII: 2G86QN327L)
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	WHITE, PINK	Score	no score
Shape	CAPSULE	Size	14mm
Flavor		Imprint Code	AP;020
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70677-0010-1	100 in 1 BOTTLE	11/25/2016
1		1 in 1 CARTON; 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	11/25/2016

Labeler - Mckesson (177667227)