Ssssting Stop Gel

Manufacturer
Schwabe Mexico, S.A. de C.V.
Effective date
2025-11-18
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:35:15

Label at a glance#

ProductSsssting Stop Gel
Active ingredientEchinacea Angustifolia, Ledum Palustre Twig, Urtica Dioica
Label structure12 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Echinacia angustifolia 1X

Ledum palustre 2X

Urtica dioica 1X

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carbomer

Citronella Oil

Ethyl Alcohol

Eucalyptus Oil

Jojoba Oil

Purified Water

Sodium Hydroxide

Witch Hazel Distillate

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Directions:

Adults and children 6 years of age and older: apply to affected area; repeat as needed.

Patch test recommended on sensitive skin.

Purpose

OTC - PURPOSE SECTION

Temporarily relieves the pain, itch, redness, and swelling of minor insect bites and stings (ants, bees, mosquitos, wasps, etc).

Soothes fever blisters and cold sores.

Indications & Usage

INDICATIONS & USAGE SECTION

Temporarily relieves the pain, itch, redness, and swelling of minor insect bites and stings (ants, bees, mosquitos, wasps, etc).

Soothes fever blisters and cold sores.

Warnings

WARNINGS SECTION

For external use only. Avoid contact with eyes and broken skin.

Do Not Use

OTC - DO NOT USE SECTION

Do not use if hypersensitive to plants in the Asteraceae (Compositae) family or any other ingredients in this product.

Breast-feeding women should not apply to breast area.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation, rash, or other allergic reaction develops, condition worsens or does not improve within 7 days.

These could be signs of a serious condition.

Pregnancy or Breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, consult a healthcare professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Overdose

OVERDOSAGE SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LHBN21825390.A01-Z-Ssssting-Stop-Gel-1-oz.jpgLHBN21825390.A01-Z-Ssssting-Stop-Gel-1-oz.jpg

LHT21825390.A01-Z-Ssssting-Stop-Gel-1-oz.jpgLHT21825390.A01-Z-Ssssting-Stop-Gel-1-oz.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130308078253909GTIN-13: 0308078253909
EAN-13: 0308078253909
GTIN-12: 308078253909
UPC-A: 308078253909
GTIN storage (14 digits): 00308078253909
LHBN21825390.A01-Z-Ssssting-Stop-Gel-1-oz.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68466-2006-4Ssssting Stop Gel28 g in 1 TUBEGEL288
68466-2006-4Ssssting Stop Gel1 in 1 CARTONGEL18
68466-2006-8Ssssting Stop Gel78 g in 1 TUBEGEL788
68466-2006-8Ssssting Stop Gel1 in 1 CARTONGEL18

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68466-200668466-2006-8, 68466-2006-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
Ssssting Stop GelECHINACEA ANGUSTIFOLIA, LEDUM PALUSTRE TWIG, URTICA DIOICA,Schwabe Mexico, S.A. de C.V.dfb2d5c4-b4d4-4252-af36-810a8354afb22025-11-18WarningsExact identifier
ndc (package): 68466-2006-8
ndc (package): 68466-2006-4
ndc (product): 68466-2006
ndc11 (package): 68466200608
ndc11 (package): 68466200604
spl id: 06f7a732-fa32-41b7-99af-ca44197cb339
spl set id: dfb2d5c4-b4d4-4252-af36-810a8354afb2

Reported adverse events (FAERS/openFDA)#

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