Indications and uses
Temporarily alleviates itching associated with minor skin irritation, inflammation and rashes due to: Eczema , Poison ivy, oak and sumac Cosmetics Psoriasis Soaps and detergents Jewelry Insect bites Seborrheic dermatitis
NeilMed Anti-Itch Spray
- Manufacturer
- NeilMed Pharmaceuticals Inc. | NeilMed Pharmaceuticals, Inc.
- Effective date
- 2024-01-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 00:07:04
Label at a glance#
ProductNeilMed Anti-Itch
Active ingredientHYDROCORTISONE
Label structure8 sections
Dosage and administration
Shake well – 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 – to apply to face, spray into palm of hand and gently apply
Label contents#
Full prescribing information#
Directions:
Shake well – 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 – to apply to face, spray into palm of hand and gently apply
Warnings:
For external use only.
Flammable: Do not use while smoking or near heat or flame
Do not use: In or near the eyes; for diaper rash ask a doctor. In case of an accidental exposure rinse with water or saline immediately, remove contact lenses and seek medical help for any persistent symptoms. Use only as directed. Do not puncture or incinerate. Contents under pressure. Avoid long term storage above 104°F. Do not store at temperatures above 120°F
Ask a doctor before use if you are using any other hydrocortisone or corticosteroid product.
Stop use and ask doctor if condition worsens or does not improve within 7 days, or clears up and occurs again within a few days.
Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.
Inactive Ingredients:
Citric Acid, Disodium EDTA, Glycerin,Poloxamer 407, Polysorbate 20, SD Alcohol 40-B,USP grade purified Water.
Uses:
Temporarily alleviates itching associated with minor skin irritation, inflammation and rashes due to:
- Eczema ,
- Poison ivy, oak and sumac
- Cosmetics
- Psoriasis
- Soaps and detergents
- Jewelry
- Insect bites
- Seborrheic dermatitis
Keep out of reach of children.
If swallowed, get medical help or contact a poison control center right away.
Drug Facts: Purpose
Anti-itch
Drug Facts:
Active Ingredient
Hydrocortisone 1.0%
NeilMed Anti Itch Spray
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| HYDROCORTISONE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 13709-239-01 | NeilMed Anti-Itch | 90 g in 1 CAN | SPRAY | 90 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- NeilMed Anti-Itch
- Anti-Itch Spray
- EDETATE DISODIUM
- ANHYDROUS CITRIC ACID
- ALCOHOL
- POLYSORBATE 20
- HYDROCORTISONE
- GLYCERIN
- POLOXAMER 407
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 13709-239 | 13709-239-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| POLYSORBATE 20 | 7T1F30V5YH | IACT |
| HYDROCORTISONE | WI4X0X7BPJ | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
| POLOXAMER 407 | TUF2IVW3M2 | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| NeilMed Anti-Itch | ANTI-ITCH SPRAY | NeilMed Pharmaceuticals Inc. | b3d34d9e-85d9-df4e-e053-2a95a90ac8d9 | 2024-01-11 | Warnings | 13709-239-01 13709-239 13709023901 0eb0a47d-4c98-a632-e063-6394a90a29dd b3d34d9e-85d9-df4e-e053-2a95a90ac8d9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.