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Estrogen Control

  • Diindolylmethane (DIM) is found in cruciferous vegetables
  • DIM helps “detoxify” estrogens
  • May inhibit aromatase
  • 60 Servings






Diindolylmethane (DIM) is made from indole-3-carbinol, a phytochemical found in cruciferous vegetables, such as broccoli, cabbage, and kale. DIM may help reduce the potency of estrogen, thereby decreasing estrogen-like effects, and repair DNA.


  • Aids in 2-hydroxylation, a process which decreases concentrations of more potent hydroxyestrones (a type of estrogen).*
  • May help decrease estrogen-like effects in men.*
  • May help control cycle-related difficulties in women.*


*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Supplement Facts


Ingredient Profile

Diindolylmethane (DIM)

Made from a phytonutrient found in vegetables.

  • DIM doesn’t reduce total estrogen, but shifts the estrogenic profile to one which is less estrogenic.
  • Promotes DNA repair by boosting the ATM enzyme.
  • Antioxidant.

Q: What is the best way to take DIMolish?

A: As a dietary supplement, take 1-2 serving(s) (1-2 capsules) per day.


Q: Are there any products I can stack with DIMolish?

A: Yes! For enhanced endocrine wellness, stack DIMolish with Vitamin D3.




  1. Saw, C. L. L., Cintrón, M., Wu, T. Y., Guo, Y., Huang, Y., Jeong, W. S., & Kong, A. N. T. (2011). Pharmacodynamics of dietary phytochemical indoles I3C and DIM: Induction of Nrf2‐mediated phase II drug metabolizing and antioxidant genes and synergism with isothiocyanates. Biopharmaceutics & drug disposition32(5), 289-300.
  2. Kitagawa, R., & Kastan, M. B. (2005, January). The ATM-dependent DNA damage signaling pathway. In Cold Spring Harbor symposia on quantitative biology(Vol. 70, pp. 99-109). Cold Spring Harbor Laboratory Press.
  3. Fan, S., Meng, Q., Xu, J., Jiao, Y., Zhao, L., Zhang, X., ... & Rosen, E. M. (2013). DIM (3, 3′-diindolylmethane) confers protection against ionizing radiation by a unique mechanism. Proceedings of the National Academy of Sciences110(46), 18650-18655.
  4. Jellinck, P. H., Gekforkert, P., Riddick, D. S., Okey, A. B., Michnovicz, J. J., & Bradlow, H. L. (1993). Ah receptor binding properties of indole carbinols and induction of hepatic estradiol hydroxylation. Biochemical pharmacology45(5), 1129-1136.



California’s Proposition 65 entitles California consumers to special warnings.

WARNING: Cancer and Reproductive Harm -