Walgreens ®

Walgreens ®
SPL v3
SPL
SPL Set ID 5aca3297-406f-4165-9895-c58ccffb374f
Route
TOPICAL
Published
Effective Date 2024-02-06
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Diphenhydramine (20 mg)
Inactive Ingredients
Alcohol Camphor (synthetic) Citric Acid Monohydrate Diazolidinyl Urea Glycerin Hypromellose, Unspecified Methylparaben Propylene Glycol Propylparaben Water Sodium Citrate, Unspecified Form

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2000-02-06
Description

Drug Facts

Purpose

Topical Analgesic

Medication Information

Purpose

Topical Analgesic

Description

Drug Facts

Use
  • temporarily relieves pain and itching associated with:
    • insect bites
    • minor burns
    • sunburn
    • minor cuts
    • scrapes
    • minor skin irritations
    • rashes due to poison ivy, poison oak, and poison sumac
Section 42229-5

Drug Facts

Section 50565-1

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Section 50567-7

When using this productavoid contact with eyes

Warnings

For external use only.

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
  • children under 2 years of age: ask a doctor
Do Not Use
  • on large areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth
Active Ingredient

Diphenhydramine HCl 2%

Other Information

Store at Room Temperature

Inactive Ingredients

SD alcohol 38-B, camphor, citric acid, diazolidinyl urea, glycerin, hydroxypropyl methylcellulose, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate

Ask A Doctor Before Use
  • on chicken pox
  • on measles
Stop Use and Ask A Doctor If
  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days
Principal Display Panel 103.5 Ml Tube Label

Structured Label Content

Use
  • temporarily relieves pain and itching associated with:
    • insect bites
    • minor burns
    • sunburn
    • minor cuts
    • scrapes
    • minor skin irritations
    • rashes due to poison ivy, poison oak, and poison sumac
Section 42229-5 (42229-5)

Drug Facts

Section 50565-1 (50565-1)

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Section 50567-7 (50567-7)

When using this productavoid contact with eyes

Purpose

Topical Analgesic

Warnings

For external use only.

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
  • children under 2 years of age: ask a doctor
Do Not Use (Do not use)
  • on large areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth
Active Ingredient (Active ingredient)

Diphenhydramine HCl 2%

Other Information (Other information)

Store at Room Temperature

Inactive Ingredients (Inactive ingredients)

SD alcohol 38-B, camphor, citric acid, diazolidinyl urea, glycerin, hydroxypropyl methylcellulose, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate

Ask A Doctor Before Use (Ask a doctor before use)
  • on chicken pox
  • on measles
Stop Use and Ask A Doctor If (Stop use and ask a doctor if)
  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days
Principal Display Panel 103.5 Ml Tube Label (PRINCIPAL DISPLAY PANEL - 103.5 mL Tube Label)

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

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Source: dailymed · Ingested: 2026-02-15T12:08:14.692121 · Updated: 2026-03-14T23:12:25.780176