Advanced Jellyfish Sting Kit

Manufacturer
Phillips Company
Effective date
2010-11-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:27:05

Label at a glance#

ProductAdvanced Jellyfish Sting Kit
Active ingredientzinc acetate
Label structure12 sections

Label contents#

Full prescribing information#

DRUG FACTS

OTC - ACTIVE INGREDIENT SECTION

Uses 
Temporarily protects injured or exposed skin or mucous membrane surfaces from harmful or annoying stimuli, and may help provide relief to such surfaces.  Contains surfactants to break down oily toxins.
____________________________________________________________________

Warnings
n For external use only; do not swallow.    n Keep away from children.
n Do not use in the eyes or apply over large areas of the body.
n Do not use if allergic to any ingredient listed on this label.
____________________________________________________________________

Directions
Step 1:  Wet the skin with water and apply powder to the affected area.  Step 2: Use water to wet the special cloth and use it to scrub the affected area to remove jellyfish barbs and to mix the protectant with any remaining toxins.  Step 3:  Repeat Steps 1 and 2 a minimum of three times or until stinging and pain stops.  Step 4: Seek immediate medical attention.
____________________________________________________________________

Other information   
Store at 40 to 120 degrees F.   Net contents of kit:  One special scrub cloth and one powder vial.  Net contents of powder vial:  3 mL.  This product contains no alcohol; no animal products; no biological products.
____________________________________________________________________

Inactive ingredients  
Water, calcium carbonate, sodium hypochlorite, sodium carbonate, sodium dodecylbenzene sulfonate, ascorbic acid, magnesium stearate, sorbic acid, stearic acid, diproplyene glycol, dimethyl sulfoxide, color.
____________________________________________________________________

Questions and Side effects
Report any side effects to Phillips Company, 311 Chickasaw St, Millerton, OK USA 74750
Email:  phillips@123phillips.com  

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients                            Purpose
Zinc acetate (.1% by volume)           Skin Protectant

ASK DOCTOR

OTC - ASK DOCTOR SECTION

Directions
Step 1:  Wet the skin with water and apply powder to the affected area.  Step 2: Use water to wet the special cloth and use it to scrub the affected area to remove jellyfish barbs and to mix the protectant with any remaining toxins.  Step 3:  Repeat Steps 1 and 2 a minimum of three times or until stinging and pain stops.  Step 4: Seek immediate medical attention.

DO NOT USE

OTC - DO NOT USE SECTION

Warnings
n For external use only; do not swallow.    n Keep away from children.
n Do not use in the eyes or apply over large areas of the body.
n Do not use if allergic to any ingredient listed on this label.

CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

n Keep away from children.
n Do not use in the eyes or apply over large areas of the body.
n Do not use if allergic to any ingredient listed on this label.

PURPOSE

OTC - PURPOSE SECTION


Active Ingredients                            Purpose
Zinc acetate (.1% by volume)           Skin Protectant

WHEN USING

OTC - WHEN USING SECTION

Directions
Step 1:  Wet the skin with water and apply powder to the affected area.  Step 2: Use water to wet the special cloth and use it to scrub the affected area to remove jellyfish barbs and to mix the protectant with any remaining toxins.  Step 3:  Repeat Steps 1 and 2 a minimum of three times or until stinging and pain stops.  Step 4: Seek immediate medical attention.


Store at 40 to 120 degrees F.

WARNINGS

WARNINGS SECTION

Warnings
n For external use only; do not swallow.    n Keep away from children.
n Do not use in the eyes or apply over large areas of the body.
n Do not use if allergic to any ingredient listed on this label.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION


Directions
Step 1:  Wet the skin with water and apply powder to the affected area.  Step 2: Use water to wet the special cloth and use it to scrub the affected area to remove jellyfish barbs and to mix the protectant with any remaining toxins.  Step 3:  Repeat Steps 1 and 2 a minimum of three times or until stinging and pain stops.  Step 4: Seek immediate medical attention.

USE

INDICATIONS & USAGE SECTION

Temporarily protects injured or exposed skin or mucous membrane surfaces from harmful or annoying stimuli, and may help provide relief to such surfaces.  Contains surfactants to break down oily toxins.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive ingredients
Water, calcium carbonate, sodium hypochlorite, sodium carbonate, sodium dodecylbenzene sulfonate, ascorbic acid, magnesium stearate, sorbic acid, stearic acid, diproplyene glycol, dimethyl sulfoxide, color.

Image of product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of product

image of productimage of product




DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1087779zinc acetate 0.1 % Topical PowderPSN1
1087779zinc acetate 0.001 MG/ML Topical PowderSCD1
1087779zinc acetate 0.1 % Topical PowderSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43074-114-172019-10-29C16284748780-1960f7f55-db02-8e05-e053-dbdaa90a074aDRUG FACTS
43074-114-182019-10-29C16284748780-1960f7f55-db02-8e05-e053-dbdaa90a074aDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43074-114-16Advanced Jellyfish Sting Kit3 mL in 1 VIAL, PLASTICPOWDER, FOR SUSPENSION31
43074-114-17Advanced Jellyfish Sting Kit0.003 mL in 1 APPLICATORPOWDER, FOR SUSPENSION0.0031
43074-114-18Advanced Jellyfish Sting Kit1 in 1 PACKAGE, COMBINATIONPOWDER, FOR SUSPENSION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43074-114ADVANCED JELLYFISH STING KIT (ZINC ACETATE) POWDER, FOR SUSPENSION [PHILLIPS COMPANY]1Legacy NDC, 3 package rows20110128_57a5d86e-5fa5-4bc6-9fe9-ec7d617fadfb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
zinc acetateACTIVE INGREDIENTFM5526K07A1
zincACTIVE MOIETYJ41CSQ7QDS1
ascorbic acidINACTIVE INGREDIENTPQ6CK8PD0R1
calcium carbonateINACTIVE INGREDIENTH0G9379FGK1
dimethyl sulfoxideINACTIVE INGREDIENTYOW8V9698H1
dipropylene glycolINACTIVE INGREDIENTE107L85C401
magnesium stearateINACTIVE INGREDIENT70097M6I301
sodium carbonateINACTIVE INGREDIENT45P3261C7T1
sodium dodecylbenzenesulfonateINACTIVE INGREDIENT554127163Y1
sodium hypochloriteINACTIVE INGREDIENTDY38VHM5OD1
sorbic acidINACTIVE INGREDIENTX045WJ989B1
stearic acidINACTIVE INGREDIENT4ELV7Z65AP1
waterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43074-11443074-114-16, 43074-114-18, 43074-114-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 3 · 160 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
stearic acidSTEARIC ACID4ELV7Z65APPOWDER, FOR SUSPENSION / ORAL1203 mg/5mlExact identifier — unii candidate
26 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TINJECTION / INFILTRATIONADJ PHExact identifier — unii candidate
28 equally ranked IID candidates
calcium carbonateCALCIUM CARBONATEH0G9379FGKTABLET, EXTENDED RELEASE / ORAL229.7 mgExact identifier — unii candidate
15 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30SUSPENSION, EXTENDED RELEASE / ORAL71 mgExact identifier — unii candidate
39 equally ranked IID candidates
stearic acidSTEARIC ACID4ELV7Z65APTABLET / ORAL336 mgExact identifier — unii candidate
26 equally ranked IID candidates
sorbic acidSORBIC ACIDX045WJ989BTABLET, FILM COATED / ORAL5 mgExact identifier — unii candidate
19 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET, FILM COATED, EXTENDED RELEASE / ORAL53 mgExact identifier — unii candidate
39 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30POWDER / TOPICAL104 mgExact identifier — unii candidate
39 equally ranked IID candidates
sorbic acidSORBIC ACIDX045WJ989BSYRUP / ORAL80 mgExact identifier — unii candidate
19 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30POWDER / ORAL25 mgExact identifier — unii candidate
39 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RINJECTION, SOLUTION / INFILTRATION0.2 %w/vExact identifier — unii candidate
25 equally ranked IID candidates
sorbic acidSORBIC ACIDX045WJ989BOINTMENT / TOPICAL0.1 %w/wExact identifier — unii candidate
19 equally ranked IID candidates
sorbic acidSORBIC ACIDX045WJ989BLOTION / TOPICAL4 mgExact identifier — unii candidate
19 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET, FOR SUSPENSION / ORAL131 mgExact identifier — unii candidate
39 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30RING / VAGINAL2 mgExact identifier — unii candidate
39 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TCAPSULE, EXTENDED RELEASE / ORAL6 mgExact identifier — unii candidate
28 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET, EXTENDED RELEASE / ORAL173 mgExact identifier — unii candidate
39 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TLOZENGE / ORAL500 mgExact identifier — unii candidate
28 equally ranked IID candidates
stearic acidSTEARIC ACID4ELV7Z65APTABLET, FILM COATED, EXTENDED RELEASE / ORAL120 mgExact identifier — unii candidate
26 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RCONCENTRATE / ORAL6 mg/1mlExact identifier — unii candidate
25 equally ranked IID candidates
stearic acidSTEARIC ACID4ELV7Z65APCAPSULE / ORAL90 mgExact identifier — unii candidate
26 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RINJECTION, POWDER, FOR SOLUTION / INTRAVENOUS2 mgExact identifier — unii candidate
25 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RSOLUTION / TOPICAL0.04 %w/wExact identifier — unii candidate
25 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TSOLUTION / OPHTHALMIC0.01 %w/vExact identifier — unii candidate
28 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RCAPSULE / ORAL7 mgExact identifier — unii candidate
25 equally ranked IID candidates
stearic acidSTEARIC ACID4ELV7Z65APEMULSION / TOPICALNAExact identifier — unii candidate
26 equally ranked IID candidates
sorbic acidSORBIC ACIDX045WJ989BGEL / TOPICAL2 mgExact identifier — unii candidate
19 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30DROPS / ORALNAExact identifier — unii candidate
39 equally ranked IID candidates
dipropylene glycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
3 equally ranked IID candidates
dimethyl sulfoxideDIMETHYL SULFOXIDEYOW8V9698HLOTION / TOPICAL45.5 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
dipropylene glycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
3 equally ranked IID candidates
stearic acidSTEARIC ACID4ELV7Z65APCAPSULE, EXTENDED RELEASE / ORAL64 mgExact identifier — unii candidate
26 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TINJECTION / SUBCUTANEOUSADJ PHExact identifier — unii candidate
28 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30IMPLANT / SUBCUTANEOUS0.5 mgExact identifier — unii candidate
39 equally ranked IID candidates
calcium carbonateCALCIUM CARBONATEH0G9379FGKTABLET, COATED / ORAL64.8 mgExact identifier — unii candidate
15 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30IMPLANT / INTRAVITREALNAExact identifier — unii candidate
39 equally ranked IID candidates
sorbic acidSORBIC ACIDX045WJ989BAEROSOL, FOAM / TOPICAL6 mgExact identifier — unii candidate
19 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RTABLET, FILM COATED / ORAL20 mgExact identifier — unii candidate
25 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30POWDER / RESPIRATORY (INHALATION)0.13 mgExact identifier — unii candidate
39 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TTABLET, DELAYED RELEASE / ORAL90 mgExact identifier — unii candidate
28 equally ranked IID candidates
stearic acidSTEARIC ACID4ELV7Z65APSHAMPOO / TOPICAL9.7 %w/wExact identifier — unii candidate
26 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RTABLET / ORAL80 mgExact identifier — unii candidate
25 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RTABLET, ORALLY DISINTEGRATING / ORAL2.35 mgExact identifier — unii candidate
25 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TINJECTION / INTRAVASCULARADJ PHExact identifier — unii candidate
28 equally ranked IID candidates
stearic acidSTEARIC ACID4ELV7Z65APTABLET, CHEWABLE / ORAL180 mgExact identifier — unii candidate
26 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET, CHEWABLE, EXTENDED RELEASE / ORAL9 mgExact identifier — unii candidate
39 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TTABLET / SUBLINGUAL8 mgExact identifier — unii candidate
28 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30TABLET, CHEWABLE / ORAL127 mgExact identifier — unii candidate
39 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RCAPSULE, EXTENDED RELEASE / ORAL17 mgExact identifier — unii candidate
25 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TGRANULE, FOR SUSPENSION / ORAL39 mgExact identifier — unii candidate
28 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RAEROSOL, METERED / RESPIRATORY (INHALATION)0.1 %w/wExact identifier — unii candidate
25 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30CAPSULE, EXTENDED RELEASE / ORAL117 mgExact identifier — unii candidate
39 equally ranked IID candidates
sorbic acidSORBIC ACIDX045WJ989BCONCENTRATE / ORAL1 mgExact identifier — unii candidate
19 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30CAPSULE, COATED, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
39 equally ranked IID candidates
stearic acidSTEARIC ACID4ELV7Z65APOINTMENT / TOPICAL15 %w/wExact identifier — unii candidate
26 equally ranked IID candidates
magnesium stearateMAGNESIUM STEARATE70097M6I30CAPSULE, DELAYED RELEASE / ORAL1060 mgExact identifier — unii candidate
39 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TSOAP / TOPICAL0.5 %w/wExact identifier — unii candidate
28 equally ranked IID candidates
ascorbic acidASCORBIC ACIDPQ6CK8PD0RPOWDER, FOR SOLUTION / ORAL560 mgExact identifier — unii candidate
25 equally ranked IID candidates
calcium carbonateCALCIUM CARBONATEH0G9379FGKTABLET, FILM COATED / ORAL300 mgExact identifier — unii candidate
15 equally ranked IID candidates
sodium carbonateSODIUM CARBONATE45P3261C7TTROCHE / ORAL375 mgExact identifier — unii candidate
28 equally ranked IID candidates

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
94aab24d-fca0-490a-9eac-822490ac8a5457a5d86e-5fa5-4bc6-9fe9-ec7d617fadfb2010-11-12WarningsExact identifier
spl id: 94aab24d-fca0-490a-9eac-822490ac8a54
spl set id: 57a5d86e-5fa5-4bc6-9fe9-ec7d617fadfb

Reported adverse events (FAERS/openFDA)#

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