FDA.reportPublic FDA data

Crash Cream

Manufacturer
Claridei Laboratories
Effective date
2026-10-27
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-10-31 01:01:45

Label at a glance#

ProductCrash Cream
Active ingredientWHITE PETROLATUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

White Petrolatum USP (50%)

OTC - PURPOSE SECTION

Purpose

Skin Protectant

Uses

  • temporarily protects minor: cuts, scrapes, burns
  • helps relieve, prevent and temporarily protect chaged, chapped or cracked skin

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

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings

When using this product do not get into eyes

Do not use on

  • deep or punctured wounds
  • animal bites
  • serious burns

DOSAGE & ADMINISTRATION SECTION

Directions

  • for cuts, scrapes, and bums
  • Clean affected area with soap and water
  • apply frequently enoughto infected areas to prevent a scab from forming

INACTIVE INGREDIENT SECTION

Inactive ingredients

Caprylic/Capric Triglyceride, Coco-Caprylate, Hydrogenated Microcrystalline Wax, Paraffin, Euphorbia Cerifera (Candelilla) Wax, Isostearyl Isostearate, C10-30 Cholersterol/Lanosterol Esters, Glycyrhetinic Acid, Phytosphingosine, Ceramide NP, Tocopherol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Crash Cream Ointment

No Sting

Advanced Skin Protection

Net Wt 1.7oz (50g)

Crash CreamCrash Cream

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.crashcream.com/crash cream.jpg

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61387-25161387-251-01, 61387-251-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WHITE PETROLATUMB6E5W8RQJ4ACTIB
CANDELILLA WAXWL0328HX19IACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
ISOSTEARYL ISOSTEARATEIV0Z586Z4YIACT
ENOXOLONEP540XA09DRIACT
TOCOPHEROLR0ZB2556P8IACT
C10-30 CHOLESTEROL/LANOSTEROL ESTERS137SL7IL0YIACT
CERAMIDE NP4370DF050BIACT
COCO-CAPRYLATE4828G836N6IACT
PHYTOSPHINGOSINEGIN46U9Q2QIACT
PARAFFINI9O0E3H2ZEIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42025-12-15full-release2026-06-01 01:23:03
32025-12-10legacy-cache2026-10-21 17:51:24

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
46012a00-5674-700f-e063-6294a90abe8501580e8e-93f3-afeb-e063-6294a90a6cbc2025-12-15WarningsExact identifier
spl set id: 01580e8e-93f3-afeb-e063-6294a90a6cbc

Reported adverse events (FAERS/openFDA)#

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