Allure Creamy Petroleum
FDA Label NDC 52000-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Universal Distribution Center Llc for the product Allure Creamy Petroleum (NDC 52000-000). 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 allure creamy petroleum jelly, active ingredient, purpose, uses, warnings, otc - when using, otc - stop use, otc - do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Allure Creamy Petroleum Jelly


Active Ingredient

Petrolatum 30%

Purpose

Skin Protectant

Uses

  • temporarily protects minor:
    • cuts
    • scrapes
    • burns
    • temporarily protects and helps relieve chapped or cracked skin
    • helps protect from the drying effects of wind and cold weather

Warnings

For external use only.

Otc - When Using

When using this product do not get into eyes.

Otc - Stop Use

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days  or clear up and occur again within a few days

Otc - Do Not Use

Do not use on

  • deep puncture wounds
  • animal bites
  • serious burns

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

Apply as needed.

Inactive Ingredients

Aqua, Carbomer, Stearic Acid, Glyceryl Monostearate, Paraffinum Liquidum, Cetearyl Alcohol, Methylparaben, Propylparaben, Triethanolamine, Tocopheryl Acetate, Parfum

Distributed By:

Universal Distribution Center96 Distribution BLVD.Edison, NJ 08817Made in China

Allure Creamy Petroleum Jelly 7Oz (52000-000-00)

Petroleumjelly (Petroleumjelly)

Petroleumjelly (Petroleumjelly)

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