Introduction: Gibberellic acid (GA3) plays important roles in many cellular processes including promoting stem elongation, and mobilization of food reserves in grass seed germination, juvenility, and sex expression. The aim of the work: To detect the possible toxic effects of GA3 on liver and kidney histopathology and effect on indicators of oxidative stress levels. Material and Methods: Seventy-five rats were included in the study and divided into two groups of animals (50 rats in treatment group and 25 rats in recovery group). The first group (treatment group) divided into 5 equal subgroups of rats (10 rats each) which were negative control group (G0T) received only distilled water, positive control treatment subgroup (G1T) received diluted sodium hydroxide in distilled water which are vehicle for GA3, subgroup G2T received 1/10 of LD50 (630 mg/kg) of GA3, subgroup G3T received 1/20 LD50 (315 mg/kg) of GA3, and subgroup G4T received 1/40 LD50 (157 mg/kg) of GA3. Treatment groups treated with GA3 orally by gavage for 12 weeks then salvaged by decapitation. The second group (recovery group) containing 25 rats that were treated with same manner as treatment groups for 12 weeks then kept after the treatment for recovery period for 2 weeks then salvaged to detect its cumulative effect. Recovery group divided into 5 equal subgroups (5 rats in each group) which were negative control recovery group (G0R), positive control recovery subgroup (G1R), subgroup G2R, subgroup G3R, and subgroup G4T. In all subgroups, liver and kidney tissue samples were taken to measure level of hepatic MDA concentration, hepatic catalase activity and examine hepatic and renal histopathologic changes. Results: hepatic MDA was significantly increased in all treatment and recovery groups in comparison to both control groups and level was directly proportional to dose of GA3 administered. There was significant reduction in the hepatic catalase enzyme activity in all treatment groups than the control treatment group especially in the group of highest doses (G2T). After the recovery period, the hepatic catalase enzyme activity continued to drop than its level after the treatment period, especially in the group (G2R). Histopathological examination revealed marked necrosis of tissues of, and the recovery period couldn't restore these pathological changes due to the cumulative effects of GA3 on the liver and kidneys. Conclusion and recommendation: GA3 possess risk to human health due to oxidative damage to tissues such as liver and kidney. Use of GA3 should be cautious, and its level in agricultural products should be regularly controlled.