Regular Strength Sleep-Aid description, usages, side effects, indications, overdosage, supplying and lots more!

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Regular Strength Sleep-Aid

WOONSOCKET PRESCRIPTION CENTER,INCORPORATED

CVS 44-189


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION




Do not use

  • in children under 12 years of age
  • 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

  • avoid alcoholic drinks

Stop use and ask a doctor if

  • sleeplessness persists continuously for more than 2 weeks.  Insomnia may be a symptom of a serious underlying medical illness.

If pregnant or breast-feeding,


Keep out of reach of children.


  • adults and children 12 years and older; take 2 tablets at bedtime if needed or as directed by a doctor
  • children under 12 years: do not use
  • see end flap for expiration date and lot number
  • store at controlled room temperature 15º-30ºC (59º-86ºF)

Principal Display Panel

CVS®
pharmacy

Compare to the active ingredient in Sominex® Original Formula*

Regular Strength
SLEEP-AID
TABLETS, 25 mg
DIPHENHYDRAMINE HCl

• Wake Rested and Refreshed
• Doctor-Preferred Sleep Ingredient

NOT FOR HOUSEHOLDS WITH YOUNG CHILDREN

72 Tablets

*This product is not manufactured or distributed by GlaxoSmithKline Consumer Healthcare, owner of the registered trademark Sominex® Tablets.
50844        REV0410B18923

Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
©2011 CVS/pharmacy
www.cvs.com        1-800-shop-CVS

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN, OR SHOWS ANY SIGNS OF TAMPERING

Regular Strength Sleep-Aid
CVS 44-189

Regular Strength Sleep-Aid

Diphenhydramine HCl TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59779-999
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 25 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS
FD&C BLUE NO. 1
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
BLUE 10 mm 44;189 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 72 in 1 BLISTER PACK
2 NDC:59779-999-23 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 1992-12-25


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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