ALRA THERAPY- allantoin lotion

ALRA THERAPY by

Drug Labeling and Warnings

ALRA THERAPY by is a Otc medication manufactured, distributed, or labeled by NEUE COSMETIC COMPANY INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

ALLANTOIN 0.5%

PURPOSE

SKIN PROTECTANT

USES

HELPS PREVENT AND RELIEVE SKIN IRRITATION, REDNESS AND PAIN, SUCH AS SYMPTOMS CAUSED BY RADIATION THERAPY OR DERMATOLOGICAL PROCEDURES.

WARNINGS

FOR EXTERNAL USE ONLY

WHEN USING

WHEN USING THIS PRODUCT

• DO NOT GET INTO EYES

STOP USE

STOP USE AND ASK A DOCTOR IF

• CONDITIONS WORSEN
• SYMPTOMS LAST MORE THAN 7 DAYS OR CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS

DO NOT USE

DO NOT USE ON

• DEEP OR PUNCTURE WOUNDS
• ANIMAL BITES
• SERIOUS BURNS

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

APPLY A SMALL AMOUNT OF ALRA THERAPY LOTION TO THE AFFECTED AREA TWICE DAILY OR AS DIRECTED BY PHYSICIAN.

INACTIVE INGREDIENTS

100% ALOE VERA (NO WATER), LANOLIN OIL, ACETYLATED LANOLIN, ISOPROPYL LANOLATE, GLYCEROL STEARATE, PEG-100 STEARATE, SOLUBLE COLLAGEN, STEARIC ACID, CETYL ALCOHOL, STEARYL ALCOHOL, TOCOPHERYL ACETATE, METHYLPROPANEDIOL, TETRASODIUM EDTA, CAPRYLYL GLYCOL, POTASSIUM SORBATE, PHENYLPROPANOL, TRIETHANOLAMINE

QUESTIONS OR COMMENTS?

CALL 1-877-265-9092

WWW.ALRA.COM

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALRA THERAPY 
allantoin lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58894-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
LANOLIN OIL (UNII: OVV5IIJ58F)
ACETYLATED LANOLIN (UNII: 2X654GD19H)
ISOPROPYL LINOLEATE (UNII: 4MW1E9AT4H)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W)
STEARIC ACID (UNII: 4ELV7Z65AP)
CETYL ALCOHOL (UNII: 936JST6JCN)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
EDETATE SODIUM (UNII: MP1J8420LU)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PHENYLPROPANOL (UNII: 0F897O3O4M)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58894-101-11	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/14/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	06/14/2016

Labeler - NEUE COSMETIC COMPANY INC (012392107)