Active Ingredients
Benzocaine 20%
L-Menthol 1%
Sooth-a-sting Swab
FDA Label NDC 50332-0050
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hart Health for the product Sooth-a-sting (NDC 50332-0050). 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, 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
Topical Anesthetic
Uses
Temporarily relief of pain and itching associated with
- insect bites
- insect stings
Warnings
For external use only
- do not get in eyes
- not for prolonged use
Allergy alert: A severe allertig reaction to insect bites and stings may require life support measures. In such cases, immediately call 911 or your local emergency provider.
Do Not Use
- in or near the eyes or over large portions of the body
- more than 3-4 times daily
Stop Use And Ask A Doctor If
- condition persists
- unusual redness, swelling, rash, or irritation occurs
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away 1-800-222-1222
Directions
- remove stinger carefully
- reverse cardboard sleeve
- crush tube between thumb and forefinger to release fluid
- apply on and aroundpoint of insect puncture
- do not reuse swab
- dispose of swab properly
Inactive Ingredient
D&C green dye#5, D&C yellow dye #10, FD&C blue dye #1, PEG 300 NF, isopropyl alcohol, purified water USP
Package Label.Principal Display Panel
0440_sooth_swabs_unit_v20f.jpg (0440 Sooth Swabs Unit V20f)
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