ALLERGY ATTACK RELIEF TO GO- diphenhydramine hydrochloride powder

Allergy Attack Relief to Go by

Drug Labeling and Warnings

Allergy Attack Relief to Go by is a Otc medication manufactured, distributed, or labeled by Breakthrough Products Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (per powder)

Diphenhydramine HCl 25mg

Purpose

Antihistamine

Uses

Temporarily relieves these symptoms due to hay fever and other upper respiratory allergies:

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

Temporarily relieves these symptoms due to common cold:

• runny nose
• sneezing

Warnings

Do not use with any other product containing diphenhydramine, even one used on skin.

Ask a doctor before use if you have

• glaucoma
• a breathing problem such as emphysema or chronic bronchitis
• 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

• 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 right away. Do not use to make a child sleepy.

Directions

adults and children 12 years and over:

• see instructions in red box for opening packet
• place 25mg (1 powder) to 50mg (2 powders) on the tongue and swallow with or without water
• take every 4 to 6 hours
• do not take more than 300mg (12 powders) in 24 hours

children 6 to under 12 years of age:

• place 12.5mg (this dose strength is not available in this package) to 25mg (1 powder) on the tongue and swallow with or without water
• take every 4 to 6 hours
• do not take more than 150mg (6 powders) in 24 hours
• do not attempt to divide a powder in half

children under 6 years of age: do not use

Inactive ingredients

citric acid, ethylcellulose, flavor, glucose, hydroxypropyl cellulose, starch, sucralose, sucrose

Questions?

1-888-998-7436 (Mon-Fri 9AM-5PM MDT)

SPL UNCLASSIFIED SECTION

Do not use if pouch
is torn or open

distributed by
URGENT Rx®
Breakthrough Products, Inc.
Denver, CO 80202

PRINCIPAL DISPLAY PANEL - 1 Powder Packet

New!

NO
WATER
REQUIRED
POUR DIRECTLY IN MOUTH

URGENT Rx®
FAST
POWDERS ™

SEE OPENING INSTRUCTIONS ON BACK PANEL

ALLERGY
ATTACK

URGENT Rx®

RELIEF
TO-GO™

DIPHENHYDRAMINE HCl /
ANTIHISTAMINE

raspberry

distributed by UrgentRx
1 POWDER PACK

INGREDIENTS AND APPEARANCE

ALLERGY ATTACK RELIEF TO GO 
diphenhydramine hydrochloride powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51596-009
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
anhydrous citric acid (UNII: XF417D3PSL)
ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
dextrose (UNII: IY9XDZ35W2)
HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
sucralose (UNII: 96K6UQ3ZD4)
sucrose (UNII: C151H8M554)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor	RASPBERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51596-009-10	10 in 1 BOX
1		1 in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 51596-009-05	5 in 1 BOX
2	NDC: 51596-009-01	1 in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 51596-009-12	12 in 1 BOX
3		1 in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 51596-009-24	24 in 1 BOX
4		1 in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 51596-009-01	1 in 1 POUCH; 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	10/01/2012

Labeler - Breakthrough Products Inc. (962008251)