PIPETTE ECZEMA- oatmeal liquid

Pipette Eczema by

Drug Labeling and Warnings

Pipette Eczema by is a Otc medication manufactured, distributed, or labeled by Amyris, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Colloidal Oatmeal 1 %

Purpose

Skin protectant

Uses

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

eczema rashes

Warnings

• For external use only

When using this product:

• do not get into eyes

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

Keep out of reach of children.

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

Directions

• apply as needed

Other Information

Protect this product from excessive heat and direct sun.

Inactive Ingredients

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?

Call 855-747-2229

Package Labeling:73517-001-01

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Package Labeling:73517-001-06

INGREDIENTS AND APPEARANCE

PIPETTE ECZEMA 
oatmeal liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73517-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y)	OATMEAL	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SQUALANE (UNII: GW89575KF9)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GLYCERIN (UNII: PDC6A3C0OX)
SHEA BUTTER (UNII: K49155WL9Y)
CERAMIDE NP (UNII: 4370DF050B)
TOCOPHEROL (UNII: R0ZB2556P8)
PHYTATE SODIUM (UNII: 88496G1ERL)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PROPANEDIOL (UNII: 5965N8W85T)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
XANTHAN GUM (UNII: TTV12P4NEE)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73517-001-01	1 in 1 BOX	05/16/2022
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 73517-001-06	1 in 1 BOX	05/16/2022
2		177 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	05/16/2022

Labeler - Amyris, Inc (185930182)