ANDANTOL ® Jelly is indicated for sunburn insect bites, burns of the 1st. and 2nd. grade, nonsuppurative allergic dermatitis.
Hypersensitivity to the components of the formula lactation and pregnancy.
Although drowsiness is very rare (less than 1% incidence) ANDANTOL ® should not be given to people who drive vehicles and precision instruments. Also avoid alcohol or other CNS depressants.
ANDANTOL ® crosses the breast for what happens in small amounts into breast milk and may cause mild sedation in breastfed.
Use in Pregnancy and Lactation
All toxicological studies have shown that ANDANTOL ® no embryotoxic action and / or teratogenic, but the safety of its use in pregnant women has not been established. Do not administer during pregnancy and lactation.
The sedative is a side effect that occurs very infrequently (less than 1%). Other reactions that may occur include dizziness, fatigue and lassitude tinnitus paradoxically euphoria. Rarely, loss of appetite and nausea.
DRUG INTERACTIONS AND OTHER GENDER:
To date there has been no reported drug interactions between ANDANTOL ® and any other drug. However it must be associated with other CNS depressants and with alcohol.
CHANGES IN RESULTS OF LABORATORY TESTS:
Clinical experience with ANDANTOL ® through many years shows that no disturbance of laboratory parameters attributable to the drug.
PRECAUTIONS IN RELATION TO EFFECTS OF Carcinogenesis, Mutagenesis, Impairment of Fertility:
DOSAGE AND ADMINISTRATION:
Route of administration: dermal.
ANDANTOL ® Jelly:
· Children over 6 years and adults: As the case may apply a very thin layer on the affected area every 6 hours.
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