JOCK BLOCK

Manufacturer
King-Tech Industry, Inc.
Effective date
2026-07-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
weekly-update
Hydrated at
2026-07-17 21:43:10

Label at a glance#

ProductJOCK BLOCK
Active ingredientSULFUR
Label structure10 sections

Indications and uses

Temporary relief of: jock itch, athlete's foot, ringworm. Also helps relieve minor skin irritation and itching.

Dosage and administration

Clean and dry affected area Shake well before use Spray from 4-6 inches away Apply 2-3 times daily For jock itch/ringworm: use for 2 weeks For athlete's foot: use for 4 weeks

Label contents#

Full prescribing information#

Active ingredient (per mL)

OTC - ACTIVE INGREDIENT SECTION

Sulfur 6X HPUS

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

Temporary relief of: jock itch, athlete's foot, ringworm. Also helps relieve minor skin irritation and itching.

Warnings

WARNINGS SECTION

For external use only

Do not use

  • on children under 2 years of age unless directed by a doctor

When using this product

  • avoid contact with the eyes

Stop use and ask a doctor if

  • irritation occurs
  • there is no improvement within 4 weeks (athlete's foot/ringworm) or 2 weeks (jock itch)

If pregnant or breast-feeding,ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 1-800-222-1222

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean and dry affected area
  • Shake well before use
  • Spray from 4-6 inches away
  • Apply 2-3 times daily
  • For jock itch/ringworm: use for 2 weeks
  • For athlete's foot: use for 4 weeks

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water, tea seed oil

Other information

DRUG INTERACTIONS SECTION

  • Store in a cool, dry place
  • HPUS = Homeopathic Pharmacopoeia of the United States

Questions or comments? Call 1-858-646-0700 or visit getjockblock.com

Homeopathic Disclaimer

SPL UNCLASSIFIED SECTION

Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Manufactured by: King-Tech Industry, Inc., 4455 Murphy Canyon Rd, Suite 208, San Diego, CA 92123

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 87627-001-00

JOCK BLOCK

Stops the Ouch

For Itch · Chafe · Fungus

Topical Sulfur Spray

Jock itch · Athlete's foot · Ringworm

Homeopathic OTC

100 mL (3.4 fl oz) jockblock_100ml_labeljockblock_100ml_label

NDC 87627-001-02 · 20 mL (0.68 fl oz)

jockblock_20ml_labeljockblock_20ml_label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130612461267627GTIN-13: 0612461267627
EAN-13: 0612461267627
GTIN-12: 612461267627
UPC-A: 612461267627
GTIN storage (14 digits): 00612461267627
jockblock_100ml_label.jpg

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87627-00187627-001-00, 87627-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMELLIA OILT1PE06G0VEIACT
WATER059QF0KO0RIACT
SULFUR70FD1KFU70ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-06-04daily-update2026-06-11 05:10:17

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
JOCK BLOCKSULFURKing-Tech Industry, Inc.6c368442-d7a5-4df8-9ed0-9e04c62b2be62026-07-02WarningsExact identifier
ndc (package): 87627-001-00
ndc (package): 87627-001-02
ndc (product): 87627-001
ndc11 (package): 87627000100
ndc11 (package): 87627000102
spl id: 55a37705-3d25-30fc-e063-6394a90ad1e6
spl set id: 6c368442-d7a5-4df8-9ed0-9e04c62b2be6

Reported adverse events (FAERS/openFDA)#

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