FDA.reportPublic FDA data

Medi ♥ First Extra Strength Itch Relief

Manufacturer
Unifirst First Aid Corporation | Medique Products
Effective date
2026-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-15 00:32:57

Label at a glance#

ProductMedi First Extra Strength Itch Relief
Active ingredientZINC ACETATE, DIPHENHYDRAMINE HYDROCHLORIDE
Label structure14 sections

Indications and uses

Uses Temporary relievies pain and itching associated with: insect bites minor burns sunburn minor skin irritations minor cuts scrapes rashes due to poison ivy, poison oak and poison sumac Dries the oozing and weeping of poison ivy, poison oak, and poison sumac

Dosage and administration

Directions do not use more than directed adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily for children under 2 years of age: do not use, consult a doctor

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Diphenhydramine Hydrochloride 2%

Zinc Acetate 0.1%

Purpose

OTC - PURPOSE SECTION

Purpose

Topical Analgesic

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

Uses

  • Temporary relievies pain and itching associated with:
  • insect bites
  • minor burns
  • sunburn
  • minor skin irritations
  • minor cuts
  • scrapes
  • rashes due to poison ivy, poison oak and poison sumac
  • Dries the oozing and weeping of poison ivy, poison oak, and poison sumac

Warnings

WARNINGS SECTION

Warnings

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use

  • on large areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use

OTC - ASK DOCTOR SECTION

Ask a doctor before use

  • on chicken pox
  • on measles

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens or does not improve withn 7 days
  • symptoms persist for more than 7 days or clear up and occur again within a few days

Keep our of reach of children

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

  • do not use more than directed
  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
  • for children under 2 years of age: do not use, consult a doctor

Other information

OTHER SAFETY INFORMATION

Other information

  • Store between 15°-30° *(59°-86°F)
  • Lot No. & Exp Date: See box or crimp of tube.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients

Carbomer homopolymer type C, cetyl alcohol, glycerin, glyceryl monostearate, light mineral oil, methyparaben, polysorbate 60, proplyparaben, purified water, stearic acid

Questions or comments?

OTC - QUESTIONS SECTION

Questions or comments? Call 1-800-635-7680

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Medi ♥ First

Topical Solutions

healingmade easy

NDC #47682-865-29

  • Histamine Blocker

Extra Strength Itch Relief

Temporary relief from pain and itching caused by

insect bites, minoir burns, sunburn, rashes due to

poison ivy, oak, sumac and more

*Compare to the

Active Ingredients

in Extra Strength

Benadryl® Cream

58429 Anti-Itch Cream 1-29-2658429 Anti-Itch Cream 1-29-26

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130347682584290GTIN-13: 0347682584290
EAN-13: 0347682584290
GTIN-12: 347682584290
UPC-A: 347682584290
GTIN storage (14 digits): 00347682584290		58429 Anti-Itch Cream 1-29-26.jpg

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47682-86547682-865-29, 47682-865-70

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYLPARABENA2I8C7HI9TIACT
POLYSORBATE 60CAL22UVI4MIACT
PROPYLPARABENZ8IX2SC1OHIACT
ZINC ACETATEFM5526K07AACTIM
CARBOMER HOMOPOLYMER TYPE C4Q93RCW27EIACT
CETYL ALCOHOL936JST6JCNIACT
GLYCERINPDC6A3C0OXIACT
DIPHENHYDRAMINE HYDROCHLORIDETC2D6JAD40ACTIB
GLYCERYL MONOSTEARATE230OU9XXE4IACT
LIGHT MINERAL OILN6K5787QVPIACT
STEARIC ACID4ELV7Z65APIACT

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
Medi First Extra Strength Itch ReliefDIPHENHYDRAMINE, ZINC ACETATEUnifirst First Aid Corporation54614e5b-8c72-d308-e063-6294a90a405d2026-06-16WarningsExact identifier
ndc (package): 47682-865-29
ndc (package): 47682-865-70
ndc (product): 47682-865
ndc11 (package): 47682086570
ndc11 (package): 47682086529
spl id: 54616303-c022-41d2-e063-6394a90a3273
spl set id: 54614e5b-8c72-d308-e063-6294a90a405d

Reported adverse events (FAERS/openFDA)#

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