ATTENDS ADVANCED BARRIER- zinc oxide spray

Attends Advanced Barrier by

Drug Labeling and Warnings

Attends Advanced Barrier by is a Otc medication manufactured, distributed, or labeled by Purna Pharmaceuticals NV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                        Purpose

Zinc Oxide 10% ................................. Skin Protectant

PURPOSE

Attends Professional Care

Prevents. Treats. Protects. 3in1

Attends Advanced Barrier S[ray

Zinc Oxide Skin Protectant

Recommended for use on irritated or chafed skin

Convenient and easy to use Pump Spray

• No rubbing
• No staining
• No stinging

(Spanish Panel)

• Prevents diaper rash
• Treats irritated, chafed skin
• Provides protective barrier to help keep skin drier

(Spanish Section

Dermatologically Tested

Net Wt. 3.5 oz (99.2 g)

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. 

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

INDICATIONS & USAGE

Uses

• Helps treat diaper rash
• Protects chafed skin due to diaper rash
• Helps protect skin for wetness

WARNINGS

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

DOSAGE & ADMINISTRATION

Directions

• Cleanse the diaper area and allow to dry
• Shake bottle well before every use
• Change wet and soiled diapers promptly
• Spray 4-6 inches from skin. No rub in is required
• Apply product liberally as often as necessary, with each dipaer change, especially at bedtime or any time exposure to wet diapers may be prolonged

OTHER SAFETY INFORMATION

Other Information

• Store between 59-77oF (15-25oC)
• Lot No & Exp date: see bottom of bottle

Questions? Call 1-800-428-8363

Manufactured in Belgium

Distributed by: 

Attends Healthcare Products, Inc.

Greenville, NC 27834

www.Attends.com

INACTIVE INGREDIENT

Inactive Ingredients

aloe barbadensis gel, aqua, C12-15 alkyl benzoate, caprylic/capric triglyceride, cera alba, coco-caprylate/caprate, diazolidinyl urea, glycerin, L-Carnoside, magnesium sulfate, panthenol, paraffinum liquidum, parfum, PEG-30 dipolyhydroxystearate, potassium sorbate, silica, sodium benzoate, tocopherol, zinc oxide.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ATTENDS ADVANCED BARRIER 
zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62450-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	10 g  in 99 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
WHITE WAX (UNII: 7G1J5DA97F)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
GLYCERIN (UNII: PDC6A3C0OX)
CARNOSINE (UNII: 8HO6PVN24W)
MAGNESIUM SULFATE (UNII: DE08037SAB)
PANTHENOL (UNII: WV9CM0O67Z)
MINERAL OIL (UNII: T5L8T28FGP)
PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62450-002-01	99 g in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	03/06/2014

Labeler - Purna Pharmaceuticals NV (372126946)

Establishment
Name	Address	ID/FEI	Business Operations
Purna Pharmaceuticals NV		372126946	manufacture(62450-002)