FDA.reportPublic FDA data

Pipette Eczema Lotion

Manufacturer
Pipette LLC | Northwest Cosmetic Laboratories L.L.C. DBA Elevation Labs, Idaho
Effective date
2025-07-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:36:02

Label at a glance#

ProductPipette Eczema
Active ingredientOATMEAL
Label structure9 sections

Indications and uses

Temporarily protects and helps relieve minor skin irritation and itching due to:  • eczema • rashes

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Colloidal Oatmeal 1 %

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

Temporarily protects and helps relieve minor skin irritation and itching due to: 

• eczema • rashes

Warnings

WARNINGS SECTION

  • For external use only

When using this product:

OTC - WHEN USING SECTION

  • do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens 
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply as needed

Other Information

SPL UNCLASSIFIED SECTION

Protect this product from excessive heat and direct sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Squalane, Caprylic/Capric Triglyceride, Glycerin, Hydrogenated Sunflower Seed Oil Polyglyceryl-3 Esters, Hydroxystearic/Linolenic/Oleic Polyglycerides, Butyrospermum Parkii (Shea) Butter, Jojoba Esters, Ceramide NP, Tocopherol, Sodium Phytate, Hydrogenated Sunflower Seed Oil, Glyceryl Esters, Cetearyl Alcohol, Propanediol, Hydroxyacetophenone, Sodium Stearoyl Lactylate, Xanthan Gum, Ethylhexylglycerin, Potassium Sorbate, Citric Acid.

Questions or comments?

OTC - QUESTIONS SECTION

Call 855-747-2229

Package Labeling:73517-001-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter Package

Add image transcription here...

Inner PackageInner Package

Add image transcription here...

Package Labeling:73517-001-06

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package2Outer Package2Inner Package2Inner Package2

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84723-00384723-003-01, 84723-003-02, 84723-003-03, 84723-003-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SQUALANEGW89575KF9IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
GLYCERINPDC6A3C0OXIACT
SHEA BUTTERK49155WL9YIACT
CERAMIDE NP4370DF050BIACT
TOCOPHEROLR0ZB2556P8IACT
PHYTATE SODIUM88496G1ERLIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
PROPANEDIOL5965N8W85TIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
SODIUM STEAROYL LACTYLATEIN99IT31LNIACT
XANTHAN GUMTTV12P4NEEIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
OATMEAL8PI54V663YACTIB

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
398325f0-ff46-f480-e063-6294a90abff02a939145-4525-c9af-e063-6294a90a0f342025-07-09WarningsExact identifier
spl id: 398325f0-ff46-f480-e063-6294a90abff0
spl set id: 2a939145-4525-c9af-e063-6294a90a0f34

Reported adverse events (FAERS/openFDA)#

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