Allure Creamy Petroleum
FDA Label NDC 52000-000
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.
Label Section Quick Index
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:
Allure Creamy Petroleum Jelly 7Oz (52000-000-00)
* Please review the disclaimer below.