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Earthly Hemps

Received a joint FDA–FTC warning letter over delta-8 THC candies and chips in snack-style packaging

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According to U.S. Food and Drug Administration, Jul 15, 2024 · Read the source · +2 more

Where
Florida, United States
First reported
Last checked

Summary

Earthly Hemps of Cape Coral, Florida, received a joint FDA–FTC warning letter dated July 15, 2024. The FDA says it reviewed the company's website and found delta-8 THC edibles for sale, including 'Dr. Blaze THC Delta-8 Slushers', 'Doweedos Delta-8 Chips' and 'Delta-8 Weedos'. The agencies' announcement singled out the Slushers product as an example of copycat packaging, and the letter describes packaging modeled on chips and candies that are popular with children. The FDA's position is that delta-8 THC is not approved for use in conventional food, which makes the products adulterated and unlawful to sell across state lines. The FTC said marketing THC edibles this way may be an unfair practice that endangers children and asked the company to report corrective steps within 15 days. Whether the company responded or changed its product line was not verified for this entry.

What the source found

  • The FDA reviewed the earthlyhemps[.]com website.
  • Products named: Dr. Blaze THC Delta-8 Slushers, Doweedos Delta-8 Chips and Delta-8 Weedos.
  • The FDA said the products mimic snack foods commonly eaten by children.
  • The FDA considered the products adulterated under the Federal Food, Drug, and Cosmetic Act.
  • The FTC said the marketing may violate Section 5 of the FTC Act.

Products named

  • delta-8 THC candies
  • delta-8 THC chips

Timeline

  1. Joint FDA–FTC warning letter issued

  2. FDA and FTC publicly announce the second round of copycat delta-8 THC letters

Sources

  1. Regulator

    U.S. Food and Drug Administration · Jul 15, 2024

    Earthly Hemps - 674916 - 07/15/2024
  2. Regulator
  3. Regulator

Wording on this page follows the sources. Found an error? See the corrections process in our editorial policy.

Status notes

Current status not verified. No close-out letter was noted on the FDA letter page when checked in September 2026.

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