PUNCHGUNK

Manufacturer
Punch Gunk
Effective date
2023-03-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:34:55

Label at a glance#

ProductPUNCHGUNK
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

TEMPORARY RELIEF OF MINOR PAIN OF MUSCLES AND JOINTS ASSOCIATED WITH STRAINS, SPRAINS, BRUSISES, SIMPLE BACKACHE, ARTHRITIS.

Dosage and administration

ADULTS AND CHILDREN OVER 12 - APPLY GENEROUSLY TO AFFECTED AREA - DO NOT USE MORE THAN 4 TIMES DAILY

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

MENTHOL 3%   

PURPOSE

OTC - PURPOSE SECTION

TOPICAL ANALGESIC   

USES

INDICATIONS & USAGE SECTION

TEMPORARY RELIEF OF MINOR PAIN OF MUSCLES AND JOINTS ASSOCIATED

WITH STRAINS, SPRAINS, BRUSISES, SIMPLE BACKACHE, ARTHRITIS.

WARNINGS

WARNINGS SECTION

USE ONLY AS DIRECTED

- FOR EXTERNAL USE ONLY

- DO NOT USE ON WOUNDS OR DAMAGED SKIN

- DO NOT USE WITH HEATING PAD

- IF CONDITION WORSENS OR IF SYMPTOMS PERSIST FOR MORE THAN 7

   DAYS CONSULT A PHYSICIAN

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

ADULTS AND CHILDREN OVER 12

- APPLY GENEROUSLY TO AFFECTED AREA

- DO NOT USE MORE THAN 4 TIMES DAILY

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

IF SWALLOWED GET MEDICAL HELP OR CONTACT POISON CONTROL

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALLANTION, ALOE BARBADENSIS, AMINOMETHYL PROPANOL,

ARNICA MONTANA FLOWER EXTRACT, BUTYLENE GLYCOL, CENTELLA ASIATICA, CETYL ALCOHOL, DILINOLEIC ACID/

PROPANEDIOL COPOYLMER, DIMETHICONE, ETHYLHEXLGLYCERIN, FRAGRANCE, GLYCERIN, GLYCERYL STEARATE,

GLYCYRRHIZA GLABRA, HAMAMELIS VIRGINIANA, HYDROGENATED VEGETABLE GLYCERIDES, ISOPROPYL MYRISTATE,

KAOLIN, MENTHOXYPROPANEDIOL, NEOPENTYL GLYCOL DIHEPTANOATE, PHENOXYETHANOL, PIPER METHYSTICUM

EXTRACT, PHYTOSTERYL SUNFLOWERSEEDATE, PROPANEDIOL, SALIX ALBA EXTRACT, 4-TERPINEOL, URTICA DIOICA

EXTRACT, VANILLY BUTYL ETHER, WATER, XANTHAN GUM.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FRONTFRONTBACKBACK

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70379-10170379-101-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
04dd1c10-eb00-0c5b-e063-6394a90a1648f46e2b3b-58c0-4576-ba0c-60eb0a48a98b2023-09-08WarningsExact identifier
spl set id: f46e2b3b-58c0-4576-ba0c-60eb0a48a98b

Reported adverse events (FAERS/openFDA)#

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