Active Ingredient
Camphor 1.24%
Blue Star Medicated Ointment
FDA Label NDC 71687-2010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Focus Consumer Healthcare, Llc for the product Blue Star Medicated (NDC 71687-2010). 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, warnings, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
Warnings
For external use only
When using this product avoid contact with eyes
Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again with a few days
Inactive Ingredient
Benzoic acid, lanolin oil, methyl salicylate, mineral oil, parafin wax, petrolatum, salicylic acid, aloe oil extract
Indications & Usage
Use for temporarily relief of pain and itching associated with minor skin irritations.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
If swallowed, get medical help or contact: Poison Control Center right away
Otc - Purpose
Purpose
Toplcal Analgesic, Anti-itch
Dosage & Administration
- 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; Consult a doctor
* Please review the disclaimer below.
