DERMOCREM- zinc oxide cream

DERMOCREM by

Drug Labeling and Warnings

DERMOCREM by is a Otc medication manufactured, distributed, or labeled by INTERNATIONAL ETHICAL LABS, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

Active ingredient

Zinc oxide 15.25%

Purpose

Skin protectant

Uses

helps treat and prevent diaper rash

protects chafed skin due to diaper rash and helps seal out wetness

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

change wet or soiled diapers promptly

cleanse the diaper area

allow to dry

apply cream liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.

Other information

store at controlled room temperature 15° to 30°C (59° to 89°F).

in a safety seal jar. Do not use if seal is broken.

Inactive ingredients

besewax, benzyl alcohol, benzyl benzoate, benzyl cinnamate, butylated hydroxyanisole, citric acid, lanolin, lavender fragrance, linalyl acetate, liquid paraffin, microcrystalline wax, paraffin wax, propylene glycol, purified water, sodium benzoate, sorbitan sesquioleate.

Questions

1-800-981-5068

Principal Display Panel

NDC: 11025-118-14

Dermocrem
(Zinc Oxide Cream)
Skin Protectant

For the Treatment & Prevention
of Diaper Rash

Net wt 8.8 oz (250 g)

INGREDIENTS AND APPEARANCE

DERMOCREM 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11025-118
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	152.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
MINERAL OIL (UNII: T5L8T28FGP)
PARAFFIN (UNII: I9O0E3H2ZE)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
BENZYL CINNAMATE (UNII: V67O3RO97U)
YELLOW WAX (UNII: 2ZA36H0S2V)
BENZYL ALCOHOL (UNII: LKG8494WBH)
LINALYL ACETATE (UNII: 5K47SSQ51G)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
BENZYL BENZOATE (UNII: N863NB338G)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11025-118-13	125 g in 1 JAR; Type 0: Not a Combination Product	05/30/2006
2	NDC: 11025-118-14	250 g in 1 JAR; Type 0: Not a Combination Product	06/08/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	05/30/2006

Labeler - INTERNATIONAL ETHICAL LABS, INC (091176933)