Not Pot Oat Puff CBD Eczema Cream

Not Pot Oat Puff CBD Eczema by

Drug Labeling and Warnings

Not Pot Oat Puff CBD Eczema by is a Otc medication manufactured, distributed, or labeled by Blemish Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NOT POT OAT PUFF CBD ECZEMA- oatmeal cream 
Blemish Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Not Pot Oat Puff CBD Eczema Cream

Drug Facts

Active Ingredients

Colloidal Oatmeal 1.0%

Purpose

Skin Protectant

Indications

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

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

Warnings

For external use only.

When Using This Product

• 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.

If swallowed, consult physician

If pregnant or breastfeeding,

• contact physician prior to use.

Directions

• Apply as needed.

Additional Information

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

Other Ingredients

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:

NOT POT OAT PUFF CBD ECZEMA 
oatmeal cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80331-177
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y)	OATMEAL	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
SHEA BUTTER (UNII: K49155WL9Y)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CANNABIS SATIVA FLOWERING TOP (UNII: 8X454SZ22D)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CARTHAMUS TINCTORIUS FLOWER OIL (UNII: SDQ136WIM5)
CHAMOMILE (UNII: FGL3685T2X)
CUCUMBER SEED (UNII: BT3S9L53JK)
COCONUT OIL (UNII: Q9L0O73W7L)
ETHYL VANILLIN (UNII: YC9ST449YJ)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
SUNFLOWER SEED (UNII: R9N3379M4Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80331-177-00	88 mL in 1 TUBE; Type 0: Not a Combination Product	10/01/2020	10/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	10/01/2020	10/31/2023

Labeler - Blemish Inc. (117512867)

Revised: 1/2022

Document Id: d58d782a-d7bb-4749-e053-2a95a90a9f89

34390-5

Set id: 94d1ea92-0861-4f5e-95c2-612ca9618638

Version: 2

Effective Time: 20220114

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