Noxzema
FDA Label NDC 64942-1264

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 Noxzema (NDC 64942-1264). 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 other, active ingredient, purpose, uses, otc - do not use, otc - when using, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient

Triclosan 0.3%

Purpose

Antibacterial

Uses

For cleansing to decrease bacteria on skin

Otc - Do Not Use

  • For external use only. Do not use on infants under 6 months of age.

Otc - When Using

When using this product

  • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
  • Discontinue use if signs of irritation or rash appear.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Wet face. Dispense product into hands.
  • Add water and work into a lather, adding more water if necessary.
  • Massage gently onto face and neck.
  • Rinse thoroughly with water.

Inactive Ingredients

Water (Aqua, Eau), Glycerin, Myristic Acid, Stearic Acid, Palmitic Acid, Sodium Lauroyl Sarcosinate, Lauric Acid, Potassium Hydroxide, Polyquaternium-10, DMDM Hydantoin, Fragrance (Parfum), Pentasodium Pentetate, Aloe Barbadensis Leaf Juice.

Questions?

1-800-436-4361

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Principal Display Panel (6 oz Tube Label)

Principal Display Panel (6 oz Tube Label)

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