Bactimicina 788

Drug Labeling and Warnings

Drug Details [pdf]

ALLERGY RELIEF- loratadine tablet 
DLC LABORATORIES, INC

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Bactimicina 788

Active ingredient (in each tablet)

Loratadine 10mg

Purpose

Antihistamine

Uses

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

                -runny nose

                -sneezing               

                -itching of the nose and throat

                -itchy, watery eyes

Warnings

Do not use if you have ever had an allergic reaction to this

product or any of its ingredients.

Ask a doctor before use if you have liver or kidney disease.

Your doctor should determine if you need a different dose.

When using this product do not take more than directed.

Taking more than directed may cause drowsiness.

Stop use and ask a doctor if an allergic reaction to this

product occurs. Seek medical help right away.

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.

Directions

adults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hours
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other information

  • TAMPER EVIDENT: Do not use if imprinted seal under cap is missing or broken
  • store between 2˚C and 30˚C (36˚F-86˚F)
  • product of Canada
  • protect from excessive moisture

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, lactose monohydrate,

magnesium stearate, microcrystalline cellulose

Questions or Comments?

1-800-858-3889

package label

bac 788NDC: 24286-1568-1

Bactimicina Tablets

Loratadine 10 mg / Antihistamine

ALLERGY RELIEF

Original Prescription Strength

Relieves:

RUNNY NOSE

SNEEZING

ITCHY, WATERY EYES
ITCHY THROAT OR NOSE
24 Hour Relief Non-Drowsy*

#When taken as directed. See Drug Facts panel

30 Tablets

10 mg each

ALLERGY RELIEF 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 24286-1568
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
Product Characteristics
ColorwhiteScoreno score
ShapeOVALSize8mm
FlavorImprint Code LOR;10;APO
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 24286-1568-11 in 1 CARTON05/01/201612/31/2018
130 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07647105/01/201612/31/2018
Labeler - DLC LABORATORIES, INC (093351930)
Registrant - Geri-Care Pharmaceutical Corp (611196254)

Revised: 9/2019
 

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