SULISRX Pain Reliever Anti-Histamine

Manufacturer
Sephoris Pharmaceuticals, LLC | Blaine Labs, Inc. | Finecure Pharmaceuticals LTD
Effective date
2026-09-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-09-22 03:01:56

Label at a glance#

ProductSULISRx Sunburn Relief Kit
Active ingredientLIDOCAINE HYDROCHLORIDE, ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE
Label structure4 sections

Label contents#

Full prescribing information#

SULISRX Pain Reliever Anti-Histamine

SPL UNCLASSIFIED SECTION

Drug Facts - Tablets

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients (in each tablet)
Acetaminophen 325 mg
Chlorpheniramine maleate 2mg

OTC - PURPOSE SECTION

Purposes

Pain reliever / fever reducer

Antihistamine

INDICATIONS & USAGE SECTION

Pain reliever & antihistamine

DOSAGE & ADMINISTRATION SECTION

Uses

  • temporarily relieves minor aches and pains
  • temporarily reduces fever
  • temporarily relieves sneezing and runny nose

WARNINGS SECTION

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

  • more th an 4,000 mg of acetaminophen in 24 hours
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

Allergy alert: Acetaminophen may cause severe skin reactions.

If a skin reaction occurs, stop use and seek medical help right away.

OTC - DO NOT USE SECTION

Do not use

  • with any other drug containing acetaminophen (prescription or nonprescription)
  • if you are allergic to acetaminophen or chlorpheniramine maleate ask a doctor or pharmacist
  • in children under 12 years of age

OTC - ASK DOCTOR SECTION

As a doctor before use if you have

  • liver disease
  • glaucoma
  • a breathing problem such as emphysema or chronic bronchitis
  • difficulty urinating due to enlargement of the prostate gland

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are

  • taking the blood thinning drug warfarin
  • taking sedatives or tranquilizers

OTC - WHEN USING SECTION

When using this product

  • drowsiness may occur
  • excitability may occur, especially in children
  • avoid alcoholic beverages
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • pain gets worse or lasts more than 5 days (6 years of age) or 10 days (adults)
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms occur
  • if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
  • prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

INSTRUCTIONS FOR USE SECTION

Directions

  • do not take more than directed (see overdose warning)
  • children 6 and under 12 years of age: take 1 tablet every 4 to 6 hours, not to exceed 6 tablets in 24 hours, or as directed by a doctor.
  • adults and children 12 yrs and over - take 2 tablets every 4-6 hours, do not exceed 10 tablets in 24 hours, or as directed by a doctor
  • children under 6 years of age: consult a doctor

STORAGE AND HANDLING SECTION

Other information

  • store between 20° to 25°C (68° to 77°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Colloidal silicon dioxide, FD&C; Blue No. 2 aluminum lake, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, pregelatinized starch, sodium starch glycolate, stearic acid, talc, titanium dioxide

SULISRX Sunburn Relief

SPL UNCLASSIFIED SECTION

Drug Facts - Lidocaine Spray

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient
Lidocaine 2%

INDICATIONS & USAGE SECTION

Purpose

External Analgesic

DOSAGE & ADMINISTRATION SECTION

Uses

Temporarily relieves pain and itching due to

  • sunburn
  • insect bites
  • minor burns
  • minor cuts
  • scrapes
  • minor skin irritations

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product

  • avoid contact with eyes
  • if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor
  • do not use in large quantities, particularly over raw surfaces or blistered areas

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days
  • symptoms clear up and occur again within a few days
  • redness or irritation develops

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INSTRUCTIONS FOR USE SECTION

Directions

  • adults and children 2 years and older: spray affected area not more than 3-4 times daily
  • children under 2 years: ask a doctor

STORAGE AND HANDLING SECTION

Other information

  • store at 20°-25°C (68°-77°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Alcohol, Caprylyl Glycol, Disodium EDTA, Ethylhexylglycerin, Hexylene Glycol, Lactic Acid, Phenoxyethanol, Polysorbate 20, Purified Water, Sodium Hydroxide, Sodium Lactate, Strontium CHloride Hexahydrate

SPL UNCLASSIFIED SECTION

Questions or comments?

1-888-8557703 (Mon-Fri 9am - 5 pm EST)

Distributed by

Sephoris Pharmaceuticals, LLC, San Diego, CA 92121

Contains: 1 topical 2% Lidocaine HCL spray and 24 pain relief/antihistamine tablets

SULISRx Sunburn Relief Kit

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SULISRx

SUNBURN RELIEF KIT

Fast Acting

Cools & Soothes Skin

Fast Pain & Itch Relief

With 2% Lidocaine HCL

Contains: 1 topical spray and 24 tablets

SULISRx Sunburn Relief Kit PDPSULISRx Sunburn Relief Kit PDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860015945105GTIN-13: 0860015945105
EAN-13: 0860015945105
GTIN-12: 860015945105
UPC-A: 860015945105
GTIN storage (14 digits): 00860015945105
SULISRx Relief Card Rev. 1-1.jpg

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87735-00387735-003-01
87735-00187735-001-01
87735-00287735-002-01
82407-001

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-09-01daily-update2026-09-04 01:01:20

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
5a6cd8f4-e6a6-d459-e063-6294a90a55235738bb75-1599-a04f-e063-6394a90a63342026-09-01WarningsExact identifier
spl set id: 5738bb75-1599-a04f-e063-6394a90a6334

Reported adverse events (FAERS/openFDA)#

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