Kroger
FDA Label NDC 30142-900
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Kroger Co for the product Kroger (NDC 30142-900). 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 active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, 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
Purpose
Topical Anesthetic
Uses
- temporary pain relief
- helps relieve and soothes pain from sunburn, minor burns, cuts, scrapes, skin irritations and insect bites.
Warnings
For external use only
Do not use in large quantities, particularly over raw surfaces or blistered areas.
When Using This Product
- avoid contact with eyes.
Stop Use And Ask A Doctor If
- Conditions worsens or symptoms persists for more than 7 days.
- Symptoms clear up and occur again within a few days.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact a Poison Control Center right away.
Directions
- adults and children 2 years of age and older.apply to affected area not more than 3 to 4 times daily
- children under 2 years of age: do not use, ask a doctor.
Inactive Ingredients
Principal Display Panel
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