Active Ingredients
- Silicone 12.0%
- Hydrocortisone 0.5%
Scarguard Md
FDA Label NDC 64269-9903
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Scarguard Labs, Llc for the product Scarguard Md (NDC 64269-9903). 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 ingredients, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Scar ManagementAnti-Pruritic
Uses
- scar management
- for the temporary relief of itching associated with minor skin irritations, inflammation and rashes
Warnings
For external use only
Do Not Use
- on children under 2 years of age. Consult a doctor.
- on mucous membranes
When Using This Product
- avoid contact with the eyes
- use in a well ventilated area
- flammable until dry
Stop Use And Ask A Doctor If
- condition worsens
- symptoms persist for more than 7 days
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- clean affected area with mild soap and water, dry thoroughly
- brush on twice daily
- allow to dry for 1 minute before coming into contact with clothing
- reapply if peeling
- children from 2-12 years of age ask a doctor
Other Information
- store at 15° to 30° C (59° to 86°F)
- Keep bottle tightly closed or product will evaporate
Inactive Ingredients
Vitamin E, specially-formulated flexible collodion
Questions?
Call1-877-566-5935
15 Ml Carton
15 mL Carton (Scarguardmd15)
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