FDA.reportPublic FDA data

Pipette Eczema Lotion

Manufacturer
Amyris, Inc
Effective date
2022-11-03
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:49:43

Label at a glance#

ProductEczema
Active ingredientOATMEAL
Label structure7 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 aks 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

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sunlight

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.
Cetearyl Alcohol, Hydrogenated Sunflower Seed Oil Glyceryl Esters, Propanediol, Hydroxyacetophenone, Sodium Stearoyl Lactylate, Xanthan
Gum, Citric Acid, Ethylhexylglycerin, Potassium Sorbate, Ceramide NP, Sodium Phytate, Tocopherol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

eczemaUCeczemaUC

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73517-42573517-425-01, 73517-425-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SQUALANEGW89575KF9IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
GLYCERINPDC6A3C0OXIACT
SUNFLOWER SEED OIL GLYCERETH-8 ESTERS358X17CAT0IACT
12-HYDROXYSTEARIC ACID933ANU3H2SIACT
SHEA BUTTERK49155WL9YIACT
HYDROGENATED JOJOBA OIL, RANDOMIZEDQ47ST02F58IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
PROPANEDIOL5965N8W85TIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
SODIUM STEAROYL LACTYLATEIN99IT31LNIACT
XANTHAN GUMTTV12P4NEEIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CERAMIDE NP4370DF050BIACT
HEXASODIUM PHYTATEZBX50UG81VIACT
TOCOPHEROLR0ZB2556P8IACT
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
ec9769f6-68e7-7c92-e053-2a95a90a0bf625bd4368-0cb5-4396-8f26-ac0dac8e1be22022-11-03WarningsExact identifier
spl id: ec9769f6-68e7-7c92-e053-2a95a90a0bf6
spl set id: 25bd4368-0cb5-4396-8f26-ac0dac8e1be2

Reported adverse events (FAERS/openFDA)#

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