MCKESSON SKIN PROTECTANT- zinc oxide cream

McKesson Skin Protectant by

Drug Labeling and Warnings

McKesson Skin Protectant by is a Otc medication manufactured, distributed, or labeled by McKesson Medical-Surgical Inc., Central Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Zinc Oxide 5.0%

PURPOSE

Purpose

Anorectal

INDICATIONS & USAGE

Uses

Provides temporary relief of itching and discomfort in the perineal area

WARNINGS

Warnings

For external use only.

If condition worsens or does not improve within 7 days, consult a physician

Do not exceed the recommended daily dosage unless directed by a physician

In case of bleeding, consult a physician immediately

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions

When practical, clean the affected area by patting or blotting with an appropriate cleaning pad.

Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.

Apply Skin Protectant Cream externally to affected area.

INACTIVE INGREDIENT

Inactive ingredients

Purified Water, Cyclotetrasiloxane, Isopropyl Palmitate, Ethylhexyl Palmitate, Glycerin, Cyclopentasiloxane, Polyglyceryl-4 Isostearate,
Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Cetyl Dimethicone, Dimethicone, Tocopherol (Vitamin E), Zea Mays Oil, Retinyl Palmitate (Vitamin A), Cholecalciferol (Vitamin D3), Beeswax, Hydrogenated Castor Oil, Sodium Chloride, DMDM Hydantoin, Iodopropynyl Butylcarbamate

QUESTIONS

Questions? Call 1-800-777-4908

PRINCIPAL DISPLAY PANEL

NDC: 68599-5312-6

McKesson

Skin

Protectant

Cream

Contains Zinc Oxide

with Vitamins A, D, and E

NET CONTENTS

6 oz

(177 ml)

MFR # 53-23103

INGREDIENTS AND APPEARANCE

MCKESSON SKIN PROTECTANT 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68599-5312
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 4 (UNII: CZ227117JE)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
MINERAL OIL (UNII: T5L8T28FGP)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
GLYCERIN (UNII: PDC6A3C0OX)
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
DIMETHICONE (UNII: 92RU3N3Y1O)
TOCOPHEROL (UNII: R0ZB2556P8)
CORN OIL (UNII: 8470G57WFM)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
YELLOW WAX (UNII: 2ZA36H0S2V)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
METHYLPARABEN (UNII: A2I8C7HI9T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68599-5312-1	24 in 1 CASE	10/25/2018	01/16/2019
1		118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 68599-5312-2	24 in 1 CASE	10/25/2018	01/16/2019
2		207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 68599-5312-6	24 in 1 CASE	10/25/2018
3		117 mL in 1 BOTTLE, PLASTIC; 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	04/24/2014

Labeler - McKesson Medical-Surgical Inc. (023904428)