Label: NIZORAL ECZEMA RELIEF CREAM- colloidal oatmeal cream
- NDC Code(s): 55505-223-33, 55505-223-36
- Packager: Kramer Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 23, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Uses
- WARNINGS
- When using this product
- Stop use and ask a doctor if
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
-
Inactive ingredients
aloe barbadensis leaf juice, butyrospermum parksii (shea)
butter, carbomer, cetyl alcohol, cocos nucifera (coconut) oil,
dimethicone, disodium EDTA, ethylhexylglycerin, glyceryl
stearate, hydrogenated lecithin, isopropyl palmitate, PEG-40
stearate, petrolatum, phenoxyethanol, sodium hydroxide,
steareth-2, stearic acid, water, xanthan gum.
- QUESTIONS
-
PRINCIPAL DISPLAY PANEL
New
Nizoral®
Eczema
Relief Cream
COLLOIDAL OATMEAL 2%
SKIN PROTECTANT
For Eczema Prone Skin
RELIEVES
Dry, Itchy Irritated Skin
SOOTHES & HYDRATES
with Shea Butter & Aloe
PROECTS
Skin from Itching
& Irritation
HELPS STRENGTHEN
Skin Moisture Barrier
Free of Fragrance,
Steroids & Parabens
Net wt 4 oz (113 g)
Specially
formulated with:
√ Shea Butter
√ Aloe
Free of:
Ⅹ Steroids
Ⅹ Fragrances
Ⅹ Parabens
Before use, read all label
information. If you have
a drug reaction, contact
a doctor and report it by
calling:
1.800.824.4894
Distributed by:
Kramer Laboratories, Inc.
Bridgewater, NJ 08807
USA
© 2024 KRAMER
LABORATORIES, INC.
K0724
-
INGREDIENTS AND APPEARANCE
NIZORAL ECZEMA RELIEF CREAM
colloidal oatmeal creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55505-223 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Oatmeal (UNII: 8PI54V663Y) (Oatmeal - UNII:8PI54V663Y) Oatmeal 2 g in 100 g Inactive Ingredients Ingredient Name Strength Aloe Vera Leaf (UNII: ZY81Z83H0X) Shea Butter (UNII: K49155WL9Y) Carbomer Homopolymer, Unspecified Type (UNII: 0A5MM307FC) Cetyl Alcohol (UNII: 936JST6JCN) Coconut Oil (UNII: Q9L0O73W7L) Dimethicone (UNII: 92RU3N3Y1O) Edetate Disodium (UNII: 7FLD91C86K) Ethylhexylglycerin (UNII: 147D247K3P) Glyceryl Monostearate (UNII: 230OU9XXE4) Hydrogenated Soybean Lecithin (UNII: H1109Z9J4N) Isopropyl Palmitate (UNII: 8CRQ2TH63M) Peg-40 Monostearate (UNII: ECU18C66Q7) Petrolatum (UNII: 4T6H12BN9U) Phenoxyethanol (UNII: HIE492ZZ3T) Sodium Hydroxide (UNII: 55X04QC32I) Steareth-2 (UNII: V56DFE46J5) Stearic Acid (UNII: 4ELV7Z65AP) Water (UNII: 059QF0KO0R) Xanthan Gum (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55505-223-33 1 in 1 CARTON 01/01/2024 1 113 g in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:55505-223-36 2 in 1 CARTON 10/15/2025 2 113 g 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 Drug M016 01/01/2024 Labeler - Kramer Laboratories (122720675)
