CARRINGTON MOISTURE BARRIER- petrolatum cream

Carrington Moisture Barrier by

Drug Labeling and Warnings

Carrington Moisture Barrier by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Petrolatum 61%

Purpose

Skin Protectant

Uses

Temporarily protects and helps relieve

• chafed skin
• chapped skin
• cracked skin

Warnings

For External Use Only

Do not use on

• deep or puncture wounds
• animal bites
• serious burns

When using this product

• do not get into eyes

Stop use and ask a doctor if

• condition worsens
• symptoms last for more than 7 days.

Keep out of reach of children.

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

Directions

• Remove urine and fecal matter with appropriate Carrington® Cleanser, such as CarraWash™, Carrafoam Skin & Perineal Cleanser™ or CarraKlenz™
• Apply Moisture Barrier Cream to affected area.

Inactive ingredients

Aloe Barbadensis Leaf juice, Butylparaben, Lecithin, Mineral Oil, Paraffin, Propylparaben, Quaternium-15, Sodium Chloride, Water.

Package/Label Principal Display Panel

NDC: 53329-076-81

CARRINGTON®

MOISTURE BARRIER CREAM

SKIN PROTECTANT

for conditions associated with INCONTINENCE

REF CRR104040

NET WT. 3.5 OZ (99 g)

INGREDIENTS AND APPEARANCE

CARRINGTON MOISTURE BARRIER 
petrolatum cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-076
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	0.61 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
MINERAL OIL (UNII: T5L8T28FGP)
PARAFFIN (UNII: I9O0E3H2ZE)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
QUATERNIUM-15 (UNII: E40U03LEM0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-076-81	99 g in 1 TUBE; Type 0: Not a Combination Product	06/28/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	01/01/2007

Labeler - Medline Industries, Inc. (025460908)

Establishment
Name	Address	ID/FEI	Business Operations
Ultra Seal Corporation		944090448	manufacture(53329-076)