Buzz Away Sting Soothe

Manufacturer
Quantum, Inc. | Sun Deep Inc.
Effective date
2025-10-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:40:03

Label at a glance#

ProductBuzz Away Sting Soothe
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

For the temporary relief ofpain and itching

Dosage and 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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.5%

Purpose

OTC - PURPOSE SECTION

Menthol 0.5%...............Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief ofpain and itching

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product, avoiid contact with eyes.

OTC - STOP USE SECTION

Stop use and ask doctor if

• condition worsens

• symptoms last more than7 days or clear up and occuragain within a few days.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or nursing, ask a health professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Safflower Oil, Aloe Barbadensis Leaf Juice, Echinacea Purpura Extract, Propylene Glycol, Glyceryl Stearate, Nettle Extract, Rosemary Leaf Oil, Cetyl Alcohol, Clove Leaf Oil, Peppermint Oil, Sage Oil, Camphor, Citronella Oil, Stearic Acid, Tea Tree Leaf Oil, Panthenol, Triethanolamine, Carbomer, Coconut Oil, Dimethicone, Tocopherol (Vitamin E), PEG-40, Castor Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Quantum Health

Bug Bite Relief

Buzz Away

Sting Soothe

Itch & Pin Relieving Liquid

Net Contents 1 Fl Oz / 30 mL

11

22

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1812747menthol 0.5 % Topical SolutionPSN1
1812747menthol 5 MG/ML Topical SolutionSCD1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130046985509930GTIN-13: 0046985509930
EAN-13: 0046985509930
GTIN-12: 046985509930
UPC-A: 046985509930
GTIN storage (14 digits): 00046985509930
Screenshot 2025-10-20 161944.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70084-810-01Buzz Away Sting Soothe30 mL in 1 BOTTLELIQUID301

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70084-81070084-810-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Buzz Away Sting SootheMENTHOLQuantum, Inc.419e34ea-17b2-ec32-e063-6394a90a603d2025-10-20WarningsExact identifier
ndc (package): 70084-810-01
ndc (product): 70084-810
ndc11 (package): 70084081001
spl id: 419e34ea-17b3-ec32-e063-6394a90a603d
spl set id: 419e34ea-17b2-ec32-e063-6394a90a603d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.