NuNature First Aid Gel

Manufacturer
Tec Laboratories Inc
Effective date
2026-01-14
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:33:24

Label at a glance#

ProductNuNature First Aid Gel
Active ingredientBENZETHONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE
Label structure13 sections

Storage and handling

Other information Store at 59-86ºF(15-30ºC)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride 0.2%

Lidocaine Hydrochloride 2.5%

INDICATIONS & USAGE SECTION

Uses

  • ​​​First aid to help prevent infection in minor:
  • cuts
  • scrapes
  • burns
  • For the temporary relief of pain or discomfort in minor:
  • cuts
  • scrapes
  • burns

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use

  • in large quantitiies particularly over raw surfaces or blister areas

OTC - WHEN USING SECTION

When using this product

avoid contact with eyes

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • symptoms last for more than 7 days or clear up and occur again within a few days
  • conditions worsens

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

if swallowed, get medical help or contact Poison Control center right away

DOSAGE & ADMINISTRATION SECTION

Directions

  • adults and children 2 years of age and older:clean the affected area whenever possible
  • apply to affected area not more than 3 to 4 times daily
  • may be covered with a sterile bandange;if bandaged, let dry first
  • children under 2 years of age:do not use, consult a doctor

STORAGE AND HANDLING SECTION

Other information

Store at 59-86ºF(15-30ºC)

INACTIVE INGREDIENT SECTION

allantoin, aminomethyl propanol, carbomer, disodium EDTA, glycerin, polyoxyl 35 castor oil, purified water, sodium carbonate, sodium metabisulfite, tea tree oil, white thyme oil.

OTC - QUESTIONS SECTION

Questions?

Call 1-800-482-4464.Serious side effects associated with this product may be reported to this number.

OTC - PURPOSE SECTION

Topical Analgestic and First Aid Antiseptic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NuNature First Aid GelNuNature First Aid Gel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130083926121011GTIN-13: 0083926121011
EAN-13: 0083926121011
GTIN-12: 083926121011
UPC-A: 083926121011
GTIN storage (14 digits): 00083926121011
NFA .jpg
Data codeData Matrix32T01L21NFA .jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51879-211-01NuNature First Aid Gel28.3 g in 1 TUBEGEL28.35

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51879-21151879-211-01

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

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
485fda68-f205-198c-e063-6394a90af038e7641dc0-8c70-fad4-e053-2a95a90abf672026-01-14WarningsExact identifier
spl id: 485fda68-f205-198c-e063-6394a90af038
spl set id: e7641dc0-8c70-fad4-e053-2a95a90abf67

Reported adverse events (FAERS/openFDA)#

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