Tacrus (Page 2 of 2)

Overdosage

If you accidentaly swallow some ointment

If you accidentally swallow the ointment, consult your doctor or pharmacist as soon as possible. Do not try to induce Vomiting.

If you forget to use Tacrus ®

If you forget to apply the ointment at the scheduled time, do it as soon as you remember and then continue as before. If you have any further questions on the use of this product, ask your doctor or pharmacist.

How supplied

10 g packs.

30 g packs.

Storage

Do not store above 25 °C.

Keep out of the reach and sight of children.

® after the expiry date which is stated on the tube and carton after Exp. The expiry date refers to the last day of that month.

THIS IS A MEDICAMENT

  • Medicament is a product which affects your health and its consumption contrary to instructions is dangerous for you.
  • Strictly follow the doctor’s prescription, the method of use and the instruction of the pharmacist who sold the medicament.
  • The doctor and the pharmacist are experts in medicine, its benefits and risks.
  • Do not by yourself interrupt the period of treatment prescribed for you.
  • Do not repeat the same prescription without consulting your doctor.
  • Keep medicament out of reach of children.

Secondary Package 10 g

Secondary Package 10 g
(click image for full-size original)

Secondary Package 30 g

Secondary Package 30 g
(click image for full-size original)

Primary Package 30 g

Primary Package 30 g
(click image for full-size original)

Primary Package 10 g

Primary Package 10 g
(click image for full-size original)

TACRUS tacrolimus ointment
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:82160-124
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TACROLIMUS (TACROLIMUS ANHYDROUS) TACROLIMUS ANHYDROUS 30 mg in 30 g
Product Characteristics
Color white Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:82160-124-01 1 TUBE in 1 CARTON contains a TUBE
1 30 g in 1 TUBE This package is contained within the CARTON (82160-124-01)
2 NDC:82160-124-02 1 TUBE in 1 CARTON contains a TUBE
2 10 g in 1 TUBE This package is contained within the CARTON (82160-124-02)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 12/11/2014
Labeler — Pella Pharmaceuticals Co. Ltd (562370925)

Revised: 01/2023 Pella Pharmaceuticals Co. Ltd

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