FDA.reportPublic FDA data

Not Pot Oat Puff CBD Eczema Cream

Manufacturer
Blemish Inc.
Effective date
2022-01-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:16:39

Label at a glance#

ProductNot Pot Oat Puff CBD Eczema
Active ingredientOATMEAL
Label structure7 sections

Dosage and administration

Apply as needed.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Colloidal Oatmeal 1.0%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Indications

INDICATIONS & USAGE SECTION

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

  • rashes
  • eczema
  • poison ivy, oak, or sumac
  • insect bites.

Warnings

WARNINGS SECTION

For external use only.

When Using This Product

OTC - WHEN USING SECTION

  • Avoid contact with eyes
  • To avoid slipping, use mat in tub or shower
  • In some skin conditions, soaking too long may over dry 
  • If symptoms persist for more than seven days, discontinue use and consult physician

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, consult physician

If pregnant or breastfeeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • contact physician prior to use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply as needed.

Additional Information

SPL UNCLASSIFIED SECTION

Protect the product in this container from excessive heat and direct sun.

Other Ingredients

INACTIVE INGREDIENT SECTION

a-Bisabalol, Allantoin, Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), Butyrospermum Parkii (Shea) Butter, Calendula Officinalis Extract, Cannabis Sativa (Hemp) Extract, Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Oil, Chamomilla Recutita (Chamomile) Extract, Cucumis Sativus (Cucumber) Extract, Cocos Nucifera (Coconut) Oil, Emulsifying Wax NF, Ethyl Vanillin, Ethylhexylglycerin, Glucosamine Sulfate, Glycerin, Glyceryl Stearate, Glycyrrhiza Glabra (Licorice) Extract, Helianthus Annuus (Sunflower) Oil, Phenoxyethanol, Xanthan Gum.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

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
80331-17780331-177-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
SHEA BUTTERK49155WL9YIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
CANNABIS SATIVA FLOWERING TOP8X454SZ22DIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
CARTHAMUS TINCTORIUS FLOWER OILSDQ136WIM5IACT
CHAMOMILEFGL3685T2XIACT
CUCUMBER SEEDBT3S9L53JKIACT
COCONUT OILQ9L0O73W7LIACT
ETHYL VANILLINYC9ST449YJIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLUCOSAMINE SULFATE1FW7WLR731IACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
SUNFLOWER SEEDR9N3379M4ZIACT
PHENOXYETHANOLHIE492ZZ3TIACT
XANTHAN GUMTTV12P4NEEIACT
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
d58d782a-d7bb-4749-e053-2a95a90a9f8994d1ea92-0861-4f5e-95c2-612ca96186382022-01-14WarningsExact identifier
spl id: d58d782a-d7bb-4749-e053-2a95a90a9f89
spl set id: 94d1ea92-0861-4f5e-95c2-612ca9618638

Reported adverse events (FAERS/openFDA)#

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