FDA.reportPublic FDA data

Everprotex

Manufacturer
Rafael Management Inc
Effective date
2025-10-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:40:01

Label at a glance#

ProductEverprotex
Active ingredientWHITE PETROLATUM
Label structure11 sections

Storage and handling

Protect this product from excessive heat and direct sun. Store at 59–86°F (15–30°C). See attached Drug Facts image for complete labeling.

Label contents#

Full prescribing information#

Active Ingredients - See complete Drug Facts labeling (attached image).

OTC - ACTIVE INGREDIENT SECTION

White Petrolatum 52% (Skin Protectant).
See attached Drug Facts image for complete labeling.

Purpose - See complete Drug Facts labeling (attached image).

OTC - PURPOSE SECTION

Skin Protectant.
See attached Drug Facts image for complete labeling.

Indications & usage - See complete Drug Facts labeling (attached image).

INDICATIONS & USAGE SECTION

Prevention and treatment of skin irritations and excoriations caused by urinary and fecal material.
Can be used on both intact and broken skin.
Will adhere to moist, weeping wounds.
Suitable for adults, children, and babies.
See attached Drug Facts image for complete labeling.

Warnings - See complete Drug Facts labeling (attached image).

WARNINGS SECTION

For external use only.
Avoid contact with eyes.
Stop use and ask a doctor if condition worsens.
This is a personal care item and should be used by one individual only.
See attached Drug Facts image for complete labeling.

Keep out of reach of children - See complete Drug Facts labeling (attached image).

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 right away.
See attached Drug Facts image for complete labeling.

Dosage & Administration - See complete Drug Facts labeling (attached image).

DOSAGE & ADMINISTRATION SECTION

Apply as needed to affected area.
See attached Drug Facts image for complete labeling.

Storage & Handling- See complete Drug Facts labeling (attached image).

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun.
Store at 59–86°F (15–30°C).
See attached Drug Facts image for complete labeling.

Inactive Ingredients - See complete Drug Facts labeling (attached image).

INACTIVE INGREDIENT SECTION

Calcium/Sodium Maleate Methyl Vinyl Ether Copolymer, Corn Starch, Ethylparaben, Methylparaben, Phenoxyethanol, Propylparaben, Sodium Carboxymethylcellulose, Zinc Oxide.
See attached Drug Facts image for complete labeling.

Questions- ​ See complete Drug Facts labeling (attached image).

OTC - QUESTIONS SECTION

Questions or concerns?
Call 1-844-693-3853 (Mon–Fri 9 AM–5 PM CST)
www.arborparkproducts.com
See attached Drug Facts image for complete labeling.

Everprotex Skin Protectant Paste – Drug Facts Insert

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Everprotex Drug FactsEverprotex Drug Facts

Everprotex Skin Protectant Paste – 2 oz (57 g) Jar Label (Principal Display, Side, and Back Panels)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Everprotex Jar LabelEverprotex Jar Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87169-001-01Everprotex57 g in 1 JARPASTE571

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87169-00187169-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYLPARABENA2I8C7HI9TIACT
WHITE PETROLATUMB6E5W8RQJ4ACTIB
STARCH, CORNO8232NY3SJIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDK679OBS311IACT
CALCIUM/SODIUM MALEATE METHYL VINYL ETHER COPOLYMER (1000000 MW, 1900 MPA.S AT 11%)5216H1HX5FIACT
ETHYLPARABEN14255EXE39IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ZINC OXIDESOI2LOH54ZIACT
PROPYLPARABENZ8IX2SC1OHIACT

Source Document#

Source XML

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
533b308f-6ea8-3a67-e063-6394a90a7dc640d2000c-f87d-d15c-e063-6294a90ab4662026-06-01WarningsExact identifier
spl set id: 40d2000c-f87d-d15c-e063-6294a90ab466

Reported adverse events (FAERS/openFDA)#

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