PAINGEL

Manufacturer
NACOR BUSINESS GROUP LLC
Effective date
2025-11-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:40:52

Label at a glance#

ProductPAINGEL
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure14 sections

Dosage and administration

Adults and Children over 12 years of age Spray two to three pumps or as necessary to cover the affected area not more than three to four times daily. Children under 12 years of age: do not use, consult a doctor.

Storage and handling

Store tightly closed in a dry place at controlled room temperature between 59°F - 86° F (15°C - 30° C).

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 10.5%

Methyl Salicylate 30%

OTC - PURPOSE SECTION

External Analgesic

USE

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

WARNINGS SECTION

  • For external use only.
  • Do not apply to wounds or damaged skin, with a heating pad or on a child under 12 years of age.

Flammable

SAFE HANDLING WARNING SECTION

Keep away from fire or flame.

OTC - WHEN USING SECTION

  • Use only as directed.
  • Do not bandage tightly.
  • Avoid contact with eyes and mucous membranes.
  • If you experience an allergic reaction, discontinue use, and consult a doctor.
  • Do not expose the area treated with product to heat or direct sunlight.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Condition worsens.
  • Redness is present.
  • Irritation develops.
  • Symptoms persist for more than 7 days or clear up occur again within a few days.
  • You experience signs of injury, such as pain, swelling or blistering where the product was applied.

If pregnant or breast – feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help, or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years of age

Spray two to three pumps or as necessary to cover the affected area not more than three to four times daily.

Children under 12 years of age: do not use, consult a doctor.

Other information

STORAGE AND HANDLING SECTION

Store tightly closed in a dry place at controlled room temperature between 59°F - 86° F (15°C - 30° C).

INACTIVE INGREDIENT SECTION

Alcohol Denat, Water (Aqua), Glycerin, Propylene Glycol, Aloe Barbadensis (Aloe Vera) Leaf Juice.

Questions or comments?

OTC - QUESTIONS SECTION

Contact us +1-307-533-7345

PAINGEL SPRAY

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PG SPRAYPG SPRAY

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130755439009727GTIN-13: 0755439009727
EAN-13: 0755439009727
GTIN-12: 755439009727
UPC-A: 755439009727
GTIN storage (14 digits): 00755439009727
FD-04729 PAINGEL PAIN RELIEF SPRAY.jpg
QR code linkQR Codepaingelnbg.com/FD-04729 PAINGEL PAIN RELIEF SPRAY.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85110-30185110-301-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
4b1d56e0-f175-1fdb-e063-6294a90a78f942f8be56-590d-3c97-e063-6394a90ab58c2026-02-18WarningsExact identifier
spl set id: 42f8be56-590d-3c97-e063-6394a90ab58c

Reported adverse events (FAERS/openFDA)#

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