OKEEFFES WORKING HANDS ECZEMA RELIEF CREAM- colloidal oatmeal cream
The Gorilla Glue Company/O'Keeffe's Company

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O'KEEFFE'S ECZEMA RELIEF HAND CREAM

Drug Facts

Active ingredient

Colloidal oatmeal 2%

Purpose

Skin protectant

Uses

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

rashes
eczema

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

Inactive ingredients Water, Glycerin, Cetyl Alcohol, Isopropyl Myristate, Dimethicone, Aluminum Starch Octylsuccinate, Cetearyl Alcohol, Ceteareth-20, Polysilicone-11, Butyrospermum Parkii (Shea) Butter, Distearyldimonium Chloride, Panthenol, Allantoin, 1,2-Hexanediol, Caprylyl Glycol, Polyquaternium-10, Beeswax, Caesalpinia Spinosa Gum, Bisabolol, Disodium EDTA, Zingiber Officianale (Ginger) Root Extract, Glyceryl Stearate, PEG-100 Stearate, Laureth-4, Laureth-23, Laureth-12, Phenoxyethanol, Ethylhexyglycerin

OKeeffesCompany.com

Questions/Comments: 1-800-275-2718

O'Keeffe's Company

Cincinnati, OH 45241

Made in USA with Domestic and Imported Materials

O'KEEFFE'S®

WORKING HANDS CREAM

ECZEMA RELIEF

RELIEVES EXTREMELY DRY, CRACKED HANDS

Colloidal Oatmeal Skin Protectant

48 Hour Itch Relief

Dermatologist Tested

Steroid & Fragrance Free

GUARANTEED RELIEF

Net Wt. 2.0 oz. (57 g)

108706 Working Hands 2OZ

OKEEFFES WORKING HANDS ECZEMA RELIEF CREAM
colloidal oatmeal cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71564-007
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y)	OATMEAL	2 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
CAESALPINIA SPINOSA RESIN (UNII: WL3883U2PO)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
LEVOMENOL (UNII: 24WE03BX2T)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
LAURETH-4 (UNII: 6HQ855798J)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
LAURETH-12 (UNII: OAH19558U1)
YELLOW WAX (UNII: 2ZA36H0S2V)
PEG-100 STEARATE (UNII: YD01N1999R)
LAURETH-23 (UNII: N72LMW566G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GINGER (UNII: C5529G5JPQ)
SHEA BUTTER (UNII: K49155WL9Y)
ALLANTOIN (UNII: 344S277G0Z)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CETYL ALCOHOL (UNII: 936JST6JCN)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
DIMETHICONE (UNII: 92RU3N3Y1O)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
PANTHENOL (UNII: WV9CM0O67Z)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71564-007-02	57 g in 1 TUBE; Type 0: Not a Combination Product	02/21/2022	12/31/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M016	02/21/2022	12/31/2024

Labeler - The Gorilla Glue Company/O'Keeffe's Company (004251914)

Revised: 11/2025

Document Id: 44764550-54ad-869c-e063-6294a90a75af

Set id: d889a37c-ae5a-1bdd-e053-2a95a90ac7b6

Version: 3

Effective Time: 20251125

The Gorilla Glue Company/O'Keeffe's Company