Itch and Bite Relief First Aid Kit

Manufacturer
WAL-MART STORES, INC.
Effective date
2021-08-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:39:04

Label at a glance#

ProductItch and Bite Relief First Aid Kit
Active ingredientHYDROCORTISONE, DIPHENHYDRAMINE HYDROCHLORIDE
Label structure15 sections

Indications and uses

• For temporary relief of itching associated with minor skin irritations, inflammation, or rashes due to: • eczemas • insect bites • poison ivy, oak or sumac • soaps • detergents • cosmetics • jewelry • seborrheic dermatitis • psoriasis • Other uses of product should be only under the advice and supervision of a doctor.

Dosage and administration

• Apply to affected area not more than 3 to 4 times daily • Children under 2: ask a doctor

Label contents#

Full prescribing information#

Active ingredient (Hydrocortisone Cream)

OTC - ACTIVE INGREDIENT SECTION

Hydrocortisone 1.0%

Purpose(Hydrocortisone Cream)

OTC - PURPOSE SECTION

Anti-itch

Uses (Hydrocortisone cream)

INDICATIONS & USAGE SECTION

• For temporary relief of itching associated with minor skin irritations, inflammation, or rashes due to:

• eczemas

• insect bites

• poison ivy, oak or sumac

• soaps

• detergents

• cosmetics

• jewelry

• seborrheic dermatitis

• psoriasis

• Other uses of product should be only under the advice and supervision of a doctor.

Warnings(Hydrocortisone Cream)

WARNINGS SECTION

For external use only

Do not use (Hydrocortisone cream)

OTC - DO NOT USE SECTION

• in the eyes

• for treatment of diaper rash

• for feminine itching

Ask a doctor before use if you are (Hydrocortisone cream)

OTC - ASK DOCTOR SECTION

• using any other hydrocortisone product

Stop use and ask a doctor if (Hydrocortisone cream)

OTC - STOP USE SECTION

the condition worsens or lasts more than 7 days, or clears up and occurs again within a few days

Keep out of reach of children (Hydrocortisone cream)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If ingested, contact a Poison Control Center right away

Directions (Hydrocortisone cream)

DOSAGE & ADMINISTRATION SECTION

• Apply to affected area not more than 3 to 4 times daily

• Children under 2: ask a doctor

Other information (Hydrocortisone cream)

OTHER SAFETY INFORMATION

• Store at room temperature (do not freeze)

• Do not use any opened or torn packets

Inactive ingredients(Hydrocortisone cream)

INACTIVE INGREDIENT SECTION

emulsifying wax, ethanol, methylparaben, mineral oil, paraffin, petrolatum, propylparaben, purified water, white wax

Active ingredient (in each caplet)(Diphen caplet)

OTC - ACTIVE INGREDIENT SECTION

Diphenhydramine Hydrochloride 25 mg

Uses (Diphen caplet)

INDICATIONS & USAGE SECTION

Temporarily relieves these symptoms due to hay fever or other respiratory allergies

• runny nose • sneezing • itching of the nose or throat • itchy, watery eyes

Temporarily relieves these symptoms due to the common cold

• runny nose • sneezing

Warnings (Diphen caplet)

WARNINGS SECTION

Do not use

• to make children sleepy

• with any other product containing diphenhydramine, even one that is used on skin.

Ask a doctor before use if you have (Diphen caplet)

OTC - ASK DOCTOR SECTION

• a breathing problem such as emphysema or chronic bronchitis

• difficulty in urination due to enlargement of the prostate gland

• glaucoma

When using this product (Diphen caplet)

OTC - WHEN USING SECTION

• marked drowsiness may occur

• avoid alcohol beverages

• alcohol, sedatives and tranquilizers may increase the drowsiness effect

• use caution when driving a motor vehicle or operating machinery

• excitability may occur, especially in children

If pregnant or breast-feeding (Diphen caplet)

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health care professional before use.

Keep out of reach of children (Diphen caplet)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

n case of overdose, contact a physician or poison control center immediately.

Directions (Diphen caplet)

DOSAGE & ADMINISTRATION SECTION

• do not take more than directed

Adults and children (12 years and older): Take 1 to 2 caplets every 4 to 6 hours as needed. Do not take more than 12 caplets in 24 hours, or as directed by a doctor.

Children under 12 years: Do not give to children under 12 years of age.

Other information (Diphen caplet)

OTHER SAFETY INFORMATION

• each caplet may contain: calcium 25mg

• store at room temperature 59º to 86ºF (15º to 30ºC)

• protect from light

• use by expiration date on packet

• tamper-evident sealed packetsM

• do not use any opened or torn packets

Inactive ingredients (Diphen caplet)

INACTIVE INGREDIENT SECTION

carnauba wax*, colloidal silicon dioxide, croscarmellose sodium, D&C red #27, dicalcium phosphate*, hypromellose, lactose*, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate*, titanium dioxide

* may contain

First Aid Kit Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OZARK TRAIL

OUTDOOR EQUIPMENT

ITCH & BITE RELIEF

FIRST AID KIT

  • Ideal for minor insects bites and itches

9 PIECES

SEE BACK PANEL FOR KIT CONTENTS

package labelpackage label

First Aid Kit Pakcage/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OZARK TRAIL

OUTDOOR EQUIPMENT

ITCH & BITE RELIEF

FIRST AID KIT

Ideal for minor insects bites and itches

9 PIECES

SEE BACK PANEL FOR KIT CONTENTS

LABELLABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
47682-184-47EA - Each47682-1849ad23d3d-85f4-4db3-893c-a0c41ee9487012017-05-03
47682-184-64EA - Each47682-184f555f4f0-8f4c-42b5-9a60-2a44dacb1dad12023-09-05

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 46 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 · 6 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
KrogerHYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATEKroger5905a7b2-36b8-9da7-e063-6394a90a28cd2026-08-14WarningsExact identifier
ndc (package): 61010-5800-1
ndc11 (package): 61010580001
HydrocortisoneHYDROCORTISONESafetec of America, Inc.da2b3b2c-11e0-401b-bbd2-d019271d1b3d2026-08-13WarningsExact identifier
ndc (package): 61010-5800-1
ndc (product): 61010-5800
ndc11 (package): 61010580001
WalgreensDIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, LIDOCAINE HCL, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, ETHYL ALCOHOLWalgreen Co.5630f48b-404c-b847-e063-6394a90a8d8e2026-07-09WarningsExact identifier
ndc (package): 47682-167-46
ndc (package): 61010-5800-1
ndc11 (package): 61010580001
ndc11 (package): 47682016746
Care ScienceDIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, LIDOCAINE HCL, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, ETHYL ALCOHOLASO LLC562f2b2c-d234-e491-e063-6294a90a705f2026-07-08WarningsExact identifier
ndc (package): 47682-167-46
ndc (package): 61010-5800-1
ndc11 (package): 61010580001
ndc11 (package): 47682016746
Medique DiphenDIPHENHYDRAMINE HYDROCHLORIDEUnifirst First Aid Corporationb61ee2e0-2543-447d-9fc4-23363d46ce042025-09-08WarningsExact identifier
ndc (package): 47682-184-46
ndc (package): 47682-167-46
ndc (product): 47682-167
ndc (product): 47682-184
ndc11 (package): 47682016746
ndc11 (package): 47682018446
c8ad60e2-f392-9d3b-e053-2a95a90a2135912e8c82-570c-b6e6-e053-2995a90ae31a2021-08-03WarningsExact identifier
spl id: c8ad60e2-f392-9d3b-e053-2a95a90a2135
spl set id: 912e8c82-570c-b6e6-e053-2995a90ae31a

Reported adverse events (FAERS/openFDA)#

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