Dove Aerosol, Spray
FDA Label NDC 64942-1813

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Conopco, Inc. D/b/a Unilever for the product Dove (NDC 64942-1813). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding dove advanced care dry spray crystal touch 48h antiperspirant deodorant- aluminum chlorohydrate aerosol, spray, drug facts, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Keep Out Of Reach Of Children

• KEEP OUT OF REACH OF CHILDREN

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