Meijer Anti-itch Ointment 1oz 94033 ZDP
- Manufacturer
- Meijer, Inc.
- Effective date
- 2022-03-31
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:49:01
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient Purpose
Hydrocortisone 1%..............................................Anti-itch
OTC - PURPOSE SECTION
Uses
- temporarily relieves itching associated with minor skin irritations, inflammation, and rashes due to: eczema; psoriasis; cosmetics; insect bites; detergents; jewelry; soaps; seborrheic dermatitis; poison ivy, oak, sumac
- temporarily relieves external and and genital itching
- other uses of this product should only be under the advice and supervision of a doctor
WARNINGS SECTION
Warnings
For external use only
OTC - DO NOT USE SECTION
Do not use
- in the genital area if you have a vaginal discharge. Consult a doctor.
- for the treatment of diaper rash. Consult a doctor.
- more than directed unless directed by a doctor
OTC - WHEN USING SECTION
When using this product
- avoid contact with eyes
- do not put directly into the rectum by using fingers or any mechanical device or applicator
OTC - STOP USE SECTION
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, and do not begin use of any other hydrocortisone product unless you have asked a doctor
- rectal bleeding occurs
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
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 (1-800-222-1222) right away.
INDICATIONS & USAGE SECTION
Directions
- for itching of skin irritaion, inflammation, and rashes: 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
- for external anal and genital itching, adults: -when practical, clean the affected area with mild soap and warm water and rinse thoroughly -gently dry by patting or blotting with toilet tissue or a soft cloth before applying -apply to affected area not more than 3 to 4 times daily -children under 12 years of age: ask a doctor
DOSAGE & ADMINISTRATION SECTION
Other Informaion
- store at room temperature 20-25ºC (68-77ºF)
INACTIVE INGREDIENT SECTION
Inactive ingredients benzoic acid, petrolatum
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| HYDROCORTISONE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 41250-887-28 | 2025-01-30 | C162847 | 48780-1 | d6a99b39-ddbd-a426-e053-dadaa90af4c2 | Meijer Anti-itch Ointment 1oz 94033 ZDP |
| 41250-887-28 | 2022-03-31 | C162847 | 48780-1 | d6a99b39-ddbd-a426-e053-dadaa90af4c2 | Meijer Anti-itch Ointment 1oz 94033 ZDP |
| 41250-887-28 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-ddbd-a426-e053-dadaa90af4c2 | Meijer Anti-itch Ointment 1oz 94033 ZDP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 41250-887-28 | Meijer Maximum Strength Anti-itch | 28 g in 1 TUBE | OINTMENT | 28 | 2 | |
| 41250-887-28 | Meijer Maximum Strength Anti-itch | 1 in 1 CARTON | OINTMENT | 1 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Meijer Maximum Strength Anti-itch
- Hydrocortisone
- BENZOIC ACID
- PETROLATUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 41250-887 | 41250-887-28 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYDROCORTISONE | WI4X0X7BPJ | ACTIB |
| BENZOIC ACID | 8SKN0B0MIM | IACT |
| PETROLATUM | 4T6H12BN9U | 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 |
|---|---|---|---|---|---|---|
| db8ac9e8-013c-add5-e053-2a95a90aa6be | a9691590-629d-7e56-e053-2a95a90ad5a1 | 2022-03-31 | Warnings | db8ac9e8-013c-add5-e053-2a95a90aa6be a9691590-629d-7e56-e053-2a95a90ad5a1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
