Dove
FDA Label NDC 64942-1364

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 64942-1364). 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 men+care dry spray extra fresh 48h antiperspirant - aluminum chlorohydrate aerosol, spray, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, 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

Dosage & Administration

Directions

apply to underarms only

Packaging

Dovemencareextrafreshaerosolpdp (Dovemenpluscareextrafresh)

Dovemencareextrafreshaerosolpdp (Dovemenpluscareextrafresh)

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