After Burn 1.425 g/57g
2.5% Lidocaine HCl · GEL · Tender Corporation d/b/a Adventure Ready Brands
After Burn is a gel containing 2.5% lidocaine hcl at 1.425 g/57g, taken topical. Manufactured by Tender Corporation d/b/a Adventure Ready Brands.
Key Facts
- Brand Name
- After Burn
- Generic Name
- 2.5% Lidocaine HCl
- NDC Code (Product)
44224-1220- Manufacturer
- Tender Corporation d/b/a Adventure Ready Brands
- Strength
- 1.425 g/57g
- Dosage Form
- GEL
- Route
- TOPICAL
- Marketing Status
- Application #
- M017
- Marketing Start
- 11/11/2024
Recall History
GFA Production Xiamen Co. Ltd.
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
GFA Production Xiamen Co. Ltd.
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
GFA Production Xiamen Co. Ltd.
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
GFA Production Xiamen Co. Ltd.
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
GFA Production Xiamen Co. Ltd.
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
GFA Production Xiamen Co. Ltd.
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
GFA Production Xiamen Co. Ltd.
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
GFA Production Xiamen Co. Ltd.
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
GFA Production Xiamen Co. Ltd.
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
Side Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Uses For the temporary relief of pain due to minor burns, sunburns, minor cuts, scrapes, or minor skin irritations
Dosage & Administration
Directions Clean rg affected area. Adults and children 2 years of age and older apply a small amount to affected area not more than 3 times daily. Children under 2 years of age consult a doctor
Warnings
Warnings for external use only When using this product avoid contact with eyes do not use in large quantities, particularly over raw surfaces or blistered areas do not use longer than 1 week unless directed by doctor Stop Use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up and occur again within a few days. Keep out of reach of children if swallowed, get medical help or contact poisn control center right away. If in eyes flush with water for 15 minutes and call a doctor
Frequently Asked Questions
What is After Burn used for?
After Burn contains 2.5% Lidocaine HCl. It is a gel taken topical. Consult your doctor for specific uses.
Is After Burn a controlled substance?
After Burn is not classified as a controlled substance by the DEA.
What is the generic name for After Burn?
The generic name for After Burn is 2.5% Lidocaine HCl. There are no other listed brand versions of 2.5% Lidocaine HCl.
What is the NDC code for After Burn 1.425 g/57g?
The NDC (National Drug Code) for After Burn 1.425 g/57g is 44224-1220, listed by Tender Corporation d/b/a Adventure Ready Brands.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)