Indications and uses
Uses For the temporary relief of pain and itching associated with: nsect bites, minor cuts, minor burns, sunburn, scrapes, minor skin irritations, rashes due to poison ivy, poison oak, or poison sumac
ProCure Anti Itch
- Manufacturer
- Twin Med LLC
- Effective date
- 2025-07-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:13:40
Label at a glance#
ProductProCure Anti Itch
Active ingredientCAMPHOR (NATURAL)
Label structure8 sections
Dosage and administration
Directions 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: do not use, consult a physician
Label contents#
Full prescribing information#
Active Ingredient
Camphor 0.5%
Purpose
External Analgesic
Uses
Uses
For the temporary relief of pain and itching associated with: nsect bites, minor cuts, minor burns, sunburn, scrapes, minor skin irritations, rashes due to poison ivy, poison oak, or poison sumac
Warnings
Warnings
For external use only
When using this product
When using this product avoid contact with the eyes
Stop use and ask a doctor if
Stop use and ask a doctor if
- Condition worsens
- Symptoms last more than 7 days or clear up and occur again within a few days
Keep out of reach of children
Keep out of reach of children. In case of accidental ingestion contact a physician or Poison Control Center right away.
Directions
Directions
- 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: do not use, consult a physician
Inactive Ingredients
Inactive Ingredients
Carbomer, Cetostearyl Alcohol, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Imidurea, Glycol Stearate, Menthol, Mineral Oil, PEG-40 Castor Oil, Petrolatum, Phenoxyethanol, Propylene Glycol, Sodium Cetostearyl Sulfate, Sodium Hydroxide, Stearic Acid, Titanium Dioxide, Water
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55681-038-75 | ProCure Anti Itch | 222 mL in 1 BOTTLE, PUMP | LOTION | 222 | 1 |
Products#
Every source-derived product name is available through these pages.
- ProCure Anti Itch
- Camphor 0.5%
- WATER
- CETOSTEARYL ALCOHOL
- MENTHOL, UNSPECIFIED FORM
- IMIDUREA
- GLYCOL STEARATE
- MINERAL OIL
- ETHYLHEXYLGLYCERIN
- PEG-40 CASTOR OIL
- CAMPHOR (NATURAL)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
- PHENOXYETHANOL
- PETROLATUM
- SODIUM HYDROXIDE
- SODIUM CETOSTEARYL SULFATE
- DIMETHICONE, UNSPECIFIED
- PROPYLENE GLYCOL
- STEARIC ACID
- TITANIUM DIOXIDE
- EDETATE DISODIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55681-038 | 55681-038-75 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| ProCure Anti Itch | CAMPHOR 0.5% | Twin Med LLC | 3afe387c-ef42-215d-e063-6394a90a41b5 | 2025-07-28 | Warnings | 55681-038-75 55681-038 55681003875 3afe387c-ef43-215d-e063-6394a90a41b5 3afe387c-ef42-215d-e063-6394a90a41b5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.