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Armand Regular Strength Itch Stopping Cream Drug Facts

Manufacturer
Weeks & Leo | Weeks & Leo Co., Inc.
Effective date
2019-04-24
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-02 00:25:17

Label at a glance#

ProductArmand Regular Strength Itch Stopping
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE
Label structure8 sections

Indications and uses

temporarliy relieves pain and itching due to: 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 due to poison: ivy oak sumac

Dosage and administration

do not use more often than directed adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily children under 2 years: ask a doctor

Storage and handling

store at 20º C to 25º C (68º F to 77º F)

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Diphenhydramine hydrochloride 2%

Zinc acetate 0.1%

Purpose

OTC - PURPOSE SECTION

Diphenhydramine hydrochloride...............Topical anagesic

Zinc acetate..............................................Skin protectant

Uses

INDICATIONS & USAGE SECTION

temporarliy relieves pain and itching due to:

  • 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 due to poison:

  • ivy
  • oak
  • sumac

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • 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

  • on chicken pox
  • on measles

When using this product

OTC - WHEN USING SECTION

do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not use more often than directed
  • adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily
  • children under 2 years: ask a doctor

Other Information

STORAGE AND HANDLING SECTION

  • store at 20º C to 25º C (68º F to 77º F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

cetyl alcohol, diazolidinyl urea, glyceryl stearate, methylparaben, PEG-40 stearate, PEG-100 stearate, propylene glycol, propylparaben, purified water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Armand REGULAR STRENGTH ITCH Itch relief CREAM

Relieves pain from insects bites & skin irritation

Topical Analgesic

Skin Protectant

Regular strength ITCH Itch relief CREAM

compare to the active ingredients in Benadryl ® Orignial strength itch stopping cream

Relieves Pain & Itch fast

Itch stopping Cream

Armand regular strength itch stopping cream .jpgArmand regular strength itch stopping cream .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
11383-26111383-261-51

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
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
METHYLPARABENA2I8C7HI9TIACT
WATER059QF0KO0RIACT
PROPYLPARABENZ8IX2SC1OHIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PEG-40 STEARATEECU18C66Q7IACT
PEG-100 STEARATEYD01N1999RIACT
CETYL ALCOHOL936JST6JCNIACT
DIPHENHYDRAMINE HYDROCHLORIDETC2D6JAD40ACTIB
ZINC ACETATEFM5526K07AACTIM

Source Document#

Source XML · Source PDF

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
d61cc7c2-88c8-400d-e053-2a95a90ad7e78748b5f6-e04b-ec1d-e053-2a95a90a834f2022-01-21WarningsExact identifier
spl set id: 8748b5f6-e04b-ec1d-e053-2a95a90a834f

Reported adverse events (FAERS/openFDA)#

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