ZEE HYDROCREAM- hydrocortisone cream cream

Zee Hydrocream by

Drug Labeling and Warnings

Zee Hydrocream by is a Otc medication manufactured, distributed, or labeled by Cintas Corp, WaterJel Technologies. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Hydrocortisone acetate (equivalent to hydrocortisone 1.0%)

Purpose

Anti-itch cream

Uses

for temporary relief of itching due to minor skin irritations from

• insect bites
• poison ivy
• poison oak
• poison sumac
• eczema
• detergents
• soaps
• cosmetics
• jewelry

Other uses should be only under the advice and supervision of a doctor

Warnings

For external use only.

Do not use

• in the eyes
• for treatment of diaper rash

When using this product do not begin use of any other hydrocortisone product

Stop use and ask a doctor if

• symptoms last for more than 7 days
• the condition gets worse
• symptoms clear up and come back in a few days

Keep out of reach of children.

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

Directions

• adults and children over 2 years: apply to affected area not more than 3 to 4 times daily
• children under 2 years: do not use, ask a doctor

Other information

• store at room temperature
• avoid excessive heat above 40°C (104°F)

Inactive ingredients

cetyl alcohol, citric acid, diazolidinyl urea, edetate disodium, glycerin, glyceryl monostearate, methylparaben, mineral oil, polyethylene glycol, propylene glycol, propylparaben, purified water, stearic acid, trolamine

Questions?

1-800-327-2704 M-F 8am - 5pm

Principal Display Panel - 25 Count Box

Maximum Strength 

Hydrocortisone Anti-Itch 

Cream 1%

25 Packets

1/32 oz (0.9 g) Each

ZEE®

1817

TO OPEN: PULL UP & TEAR OUT

Principal Display Panel - Packet

ZEE®

Distributed by

ZEE MEDICAL

Distributors, LLC

Mason, OH 45040

Maximum Strength Hydrocortisone 

Anti-itch Cream 1%

Net Wt. 1/32 oz (0.9g) Rev 121

tear here

INGREDIENTS AND APPEARANCE

ZEE HYDROCREAM 
hydrocortisone cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42961-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE ACETATE	1 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
CETYL ALCOHOL (UNII: 936JST6JCN)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
METHYLPARABEN (UNII: A2I8C7HI9T)
MINERAL OIL (UNII: T5L8T28FGP)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
TROLAMINE (UNII: 9O3K93S3TK)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42961-015-02	25 in 1 BOX	05/05/2022
1	NDC: 42961-015-01	900 mg in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/05/2022

Labeler - Cintas Corp (056481716)

Establishment
Name	Address	ID/FEI	Business Operations
WaterJel Technologies		155522589	manufacture(42961-015)