Diphenhydramine Hydrochloride description, usages, side effects, indications, overdosage, supplying and lots more!

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Diphenhydramine Hydrochloride

Bonita Pharmaceuticals LLC
Bonita Pharmaceuticals LLC




FULL PRESCRIBING INFORMATION

Diphenhydramine HCl 25 mg

Antihistamine

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

  • runny nose
  • itchy, watery eyes
  • itching of the nose and throat
  • sneezing
  • with any other product containing diphenhydramine, even one used on skin.
  • to make a child sleepy.
  • glaucoma
  • difficulty in urinating due to an enlargement of the prostate gland
  • a breathing problem such as emphysema or chronic bronchitis

taking sedatives or tranquilizers.

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

ask a health professional before use.

Keep out of reach of children.

get medical help or contact a Poison Control Center right away. (1-800-222-1222)

  • take every 4 to 6 hours as needed
  • do not take more than 6 times in 24 hours or as directed by a doctor

Adults and children 12 years and older

  • 1 or 2 caplets (25mg to 50mg)

Children under 12 years

  • ask a doctor
  • Store at room temperature
  • keep lid tightly closed in dry place
  • Do not use if imprinted safety seal under cap is broken or missing

Croscarmellose Sodium, D&C Red #27, Dicalcium Phosphate Dihydrate, Hydroxypropyle MethylCellulose, Magnesium Stearate, Microcrystalline Cellulose, Polyethylene Glycol, Propylene Glycol, Silica, Stearic Acid and Titanium Dioxide.

If you have any questions or comments, or to report an adverse event, please contact (855) 729-7200.

Diphenhydramine Hydrochloride

Diphenhydramine Hydrochloride

Diphenhydramine Hydrochloride TABLET, COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53598-004
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
D&C RED NO. 27
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
HYPROMELLOSES
MAGNESIUM STEARATE
cellulose, microcrystalline
POLYETHYLENE GLYCOLS
propylene glycol
SILICON DIOXIDE
STEARIC ACID
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
white ((Coated with pink film)) 11 mm G17 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:53598-004-01 100 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2013-05-21


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Be sure to consult your doctor before taking any medication!
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