TUNA .1 g/mL

THUNNUS THYNNUS · INJECTION, SOLUTION · ALK-Abello, Inc.

No Recall History

Plain English

TUNA is a injection, solution containing thunnus thynnus at .1 g/mL, taken percutaneous. Manufactured by ALK-Abello, Inc..

Key Facts

Brand Name: TUNA
Generic Name: THUNNUS THYNNUS
NDC Code (Product): 0268-6226
Manufacturer: ALK-Abello, Inc.
Strength: .1 g/mL
Dosage Form: INJECTION, SOLUTION
Route: PERCUTANEOUS
Marketing Status
Application #: BLA103753
Marketing Start: 02/23/1998

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

vomiting199 reports

pruritus196 reports

condition aggravated182 reports

headache180 reports

weight decreased173 reports

drug ineffective172 reports

infection172 reports

hypertension171 reports

psoriasis171 reports

urticaria168 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Use: Helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Dosage & Administration

Directions: For Sunscreen Use Apply generously 15 minutes before sun exposure. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including. Limit time in the sun, especially from 10 a.m.-2 p.m., wear long- sleeved shirts, pants, hats and sunglasses. Children under 6 months of age: Ask a doctor. Sun Protection Measures:

Warnings

Warnings: For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Frequently Asked Questions

What is TUNA used for?

TUNA contains THUNNUS THYNNUS. It is a injection, solution taken percutaneous. Consult your doctor for specific uses.

Is TUNA a controlled substance?

TUNA is not classified as a controlled substance by the DEA.

What is the generic name for TUNA?

The generic name for TUNA is THUNNUS THYNNUS. There are no other listed brand versions of THUNNUS THYNNUS.

What is the NDC code for TUNA .1 g/mL?

The NDC (National Drug Code) for TUNA .1 g/mL is 0268-6226, listed by ALK-Abello, Inc..

Product NDC

0268-6226

Package NDC

0268-6226-06

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)