FDA.reportPublic FDA data

24/7 Life Oral Pain Relief Gel 0.5 oz (58853A)

Manufacturer
7-ELEVEN, INC.
Effective date
2025-10-31
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:41:46

Label at a glance#

Product7 Select Oral Pain Maximum Strength Relief
Active ingredientBENZOCAINE
Label structure12 sections

Storage and handling

Other information store at 20° to 25°C (68° to 77°F) this preparation is intended for use in cases of toothache, only as a temporary expedient until a dentist or doctor can be consulted do not use continuously

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                 Purpose

Benzocaine 20%.................................Oral Pain reliever

OTC - PURPOSE SECTION

Use for the temporary relief of pain due to:

  • toothache
  • canker sores
  • gum pain
  • denture pain
  • cheek bites

WARNINGS SECTION

Warnings

Methemoglobinemia warning: Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate meddical attention if you or a child in your care develops:

  • pale, gray, or blue colored skin (cyanosis)
  • headache
  • rapid heart rate
  • shortness of breath
  • dizziness or lightheadedness
  • fatigue or lack of energy

Allergy alert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics

OTC - DO NOT USE SECTION

Do not use

  • more than directed
  • for more than 7 days unless directed by a dentist or doctor
  • for teething
  • in children under 2 years of age

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • sore mouth symptoms do not improve in 7 days
  • swelling, rash or fever develops
  • irritation, pain or redness persists or worsens

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

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 (1-800-222-1222) right away.

INDICATIONS & USAGE SECTION

Directions

Adults and children 2 years of age and older.Remove cap and cut tip of tube. Apply a small amount of product to the cavity and around gum surrounding the teeth. Use up to 4 times daily or as directed by a dentist or dentist.
Children under 12 years of age.Should be supervised in the use of this product.
Children under 2 years of age.Do not use.

STORAGE AND HANDLING SECTION

Other information

  • store at 20° to 25°C (68° to 77°F)
  • this preparation is intended for use in cases of toothache, only as a temporary expedient until a dentist or doctor can be consulted
  • do not use continuously

INACTIVE INGREDIENT SECTION

Inactive ingredients glycerin, peppermint oil, polyethylene glycol 400, polyethylene glycol 4000, saccharin sodium, sorbitol

DOSAGE & ADMINISTRATION SECTION

DISTRIBUTED BY 7-ELEVEN, INC.

Irving, TX 75063

WWW.7-ELEVEN.COM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

58853A58853A

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
238910benzocaine 20 % Oral GelPSN9
238910benzocaine 0.2 MG/MG Oral GelSCD9
238910benzocaine 20 % (180-220 MG per 1 GM) Oral GelSY9

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130052548588533GTIN-13: 0052548588533
EAN-13: 0052548588533
GTIN-12: 052548588533
UPC-A: 052548588533
GTIN storage (14 digits): 00052548588533		58853A.1.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10202-853-142022-03-31C16284748780-1d6a99b39-365d-a426-e053-dadaa90af4c27 Select Oral Pain Reliever Max. Strength Gel 0.5oz (58853)
10202-853-142022-03-31C16284748780-1d6a99b39-365d-a426-e053-dadaa90af4c224/7 Life Oral Pain Relief Gel 0.5 oz (58853A)
10202-853-142022-01-28C16284748780-1d6a99b39-365d-a426-e053-dadaa90af4c27 Select Oral Pain Reliever Max. Strength Gel 0.5oz (58853)
10202-853-142022-01-28C16284748780-1d6a99b39-365d-a426-e053-dadaa90af4c224/7 Life Oral Pain Relief Gel 0.5 oz (58853A)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10202-853-147 Select Oral Pain Maximum Strength Relief14 g in 1 TUBEGEL149
10202-853-147 Select Oral Pain Maximum Strength Relief1 in 1 BLISTER PACKGEL19

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10202-85310202-853-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYETHYLENE GLYCOL 400B697894SGQIACT
POLYETHYLENE GLYCOL 40004R4HFI6D95IACT
SACCHARIN SODIUMSB8ZUX40TYIACT
SORBITOL506T60A25RIACT
BENZOCAINEU3RSY48JW5ACTIB
GLYCERINPDC6A3C0OXIACT
MINTFV98Z8GITPIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72024-12-02full-release2026-06-01 00:48:04

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
7 Select Oral Pain Maximum Strength ReliefBENZOCAINE7-ELEVEN, INC.f170a570-1c50-4b9a-be16-9b01bf5eaa742025-10-31WarningsExact identifier
ndc (package): 10202-853-14
ndc (product): 10202-853
ndc11 (package): 10202085314
spl id: 427bbea1-432f-6911-e063-6394a90a9d10
spl set id: f170a570-1c50-4b9a-be16-9b01bf5eaa74

Reported adverse events (FAERS/openFDA)#

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