INDOOR OUTDOOR ALLERGY RELIEF- loratadine tablet

Indoor Outdoor Allergy Relief by

Drug Labeling and Warnings

Indoor Outdoor Allergy Relief by is a Otc medication manufactured, distributed, or labeled by Walgreens. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Loratadine, USP 10 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

• runny nose
• sneezing
• itchy, watery eyes
• itching of the nose or throat

Warnings

Do not use

if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have

liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product,

do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor if

 an allergic reaction to this product occurs. Seek medical help right away

If pregnant or breast-feeding,

 ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222)

Directions

• adults and children 6 years and over: 1 tablet daily; not more than 1 tablet in 24 hours
• children under 6 years of age: ask a doctor
• consumers with liver or kidney disease: ask a doctor

Other information

• store at 20º-25ºC (68º-77ºF) (see UPS Controlled Room Temperature

Inactive ingredients

lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

Compare to Claritin® Tablets active ingredient††

NON-DROWSY* ORIGINAL

PRESCRIPTION STRENGTH

24 HOUR ALLERGY

LORATADINE TABLETS, 10 mg / ANTIHISTAMINE

24 HOUR TABLETS

INDOOR & OUTDOOR ALLERGIES

• 24-hour relief of sneezing, runny nose, itchy, watery eyes & itchy throat or nose

*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.

TABLETS

†This product is not manufactured or distributed by Bayer Healthcare LLC, distributor of Claritin® Tablets

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOW ANY SIGN OF TAMPERING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

walgreens.com

Package Label

WALGREENS Indoor & Outdoor Allergy Relief

INGREDIENTS AND APPEARANCE

INDOOR OUTDOOR ALLERGY RELIEF 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0858
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)	LORATADINE	10 mg

Inactive Ingredients
Ingredient Name	Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)

Product Characteristics
Color	WHITE	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	GG296
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0858-10	10 in 1 CARTON	09/30/2018
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 0363-0858-20	20 in 1 CARTON	09/30/2018
2		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC: 0363-0858-05	5 in 1 CARTON	09/30/2018
3		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
4	NDC: 0363-0858-30	1 in 1 BOX	09/30/2018
4		300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5	NDC: 0363-0858-15	1 in 1 CARTON	09/30/2018
5		150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6	NDC: 0363-0858-90	1 in 1 BOX	09/30/2018
6		90 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7	NDC: 0363-0858-70	1 in 1 BOX	09/30/2018
7		70 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
8	NDC: 0363-0858-45	1 in 1 BOX	09/30/2018
8		45 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
9	NDC: 0363-0858-03	1 in 1 BOX	09/30/2018
9		30 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
ANDA	ANDA075209	09/30/2018

Labeler - Walgreens (008965063)