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HomeHealth and Safety CodeDiv. 104Pt. 5Ch. 6Art. 3§ 111335 Drug Device Labeling Requirements

§ 111335 Drug Device Labeling Requirements

Health and Safety Code·California
AI Summary·Official Text·Key Terms·Related Statutes·References
AI SummaryVerified

§ 111335 Drug Device Labeling Requirements

Key Takeaways

  • •If a medicine or medical tool has wrong or missing info on its label or box, it's considered 'misbranded'.
  • •The label or box must follow the rules in Chapter 4 of the law.
  • •This rule helps make sure people get the right info about what they're using.

Example

You buy a painkiller at the store, but the box doesn’t say how much to take or what’s in it.

This is against the law because the box is missing important info that should be there. The store could get in trouble for selling it.

AI-generated — May contain errors. Not legal advice. Always verify source.

Official Source
View on CA.gov

§ 111335 Drug Device Labeling Requirements

Any drug or device is misbranded if its labeling or packaging does not conform to the requirements of Chapter 4 (commencing with Section 110290). (Added by Stats. 1995, Ch. 415, Sec. 6. Effective January 1, 1996.)

Last verified: January 23, 2026

Key Terms

misbrandedlabelingpackagingChapter 4Section 110290

Related Statutes

  • § 111735 Cosmetic Labeling Requirements
  • § 111385 Drug Device Deterioration Labeling
  • § 110680 Food Labeling Requirements
  • § 111330 Misbranded Drug Labeling
  • § 111345 Drug Labeling Conspicuity Requirements

References

  • Official text at leginfo.legislature.ca.gov
  • California Legislature. Health and Safety Code. Section 111335.
View Official Source