Indoor Outdoor Allergy Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Walgreens. The primary component is Loratadine.
| Product ID | 0363-0858_4d027712-63bf-4bda-bf1d-f594680788d9 | 
| NDC | 0363-0858 | 
| Product Type | Human Otc Drug | 
| Proprietary Name | Indoor Outdoor Allergy Relief | 
| Generic Name | Loratadine | 
| Dosage Form | Tablet | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2018-09-30 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA075209 | 
| Labeler Name | Walgreens | 
| Substance Name | LORATADINE | 
| Active Ingredient Strength | 10 mg/1 | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2019-12-31 | 
| Marketing Start Date | 2018-09-30 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | ANDA | 
| Application Number | ANDA075209 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075209 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075209 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075209 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075209 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075209 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075209 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075209 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-09-30 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075209 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-09-30 | 
| Ingredient | Strength | 
|---|---|
| LORATADINE | 10 mg/1 | 
| SPL SET ID: | 19fb573f-29a1-4166-becb-0698cfbb682c | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0363-0858 | Indoor Outdoor Allergy Relief | Loratadine | 
| 0363-0904 | Indoor Outdoor Allergy Relief | Fexofenadine HCl | 
| 0363-1612 | allergy relief | Loratadine | 
| 0113-7612 | Basic Care allergy relief | Loratadine | 
| 0113-7500 | basic care childrens allergy relief | loratadine | 
| 0113-7671 | Basic Care Childrens Allergy Relief | Loratadine | 
| 0121-0849 | Childrens Loratadine | LORATADINE | 
| 0363-2131 | Childrens Loratadine | Loratadine | 
| 0363-4020 | CHILDRENS LORATADINE ODT | Loratadine | 
| 0363-2092 | Childrens Wal-itin | Loratadine | 
| 0363-2108 | Childrens Walitin | Loratadine | 
| 0113-0612 | good sense allergy relief | Loratadine | 
| 0113-1191 | good sense allergy relief | loratadine | 
| 0113-1612 | good sense allergy relief | Loratadine | 
| 0113-9755 | good sense allergy relief | loratadine | 
| 0113-0671 | Good Sense childrens allergy relief | Loratadine | 
| 0113-1019 | good sense childrens allergy relief | loratadine | 
| 0113-1719 | good sense childrens allergy relief | Loratadine | 
| 0179-8317 | Loratadine | Loratadine | 
| 0363-0522 | Loratadine | Loratadine | 
| 0363-0527 | Loratadine | Loratadine | 
| 0363-0752 | Loratadine | Loratadine | 
| 0363-0699 | Wal itin | Loratadine | 
| 0363-0754 | Wal-itin | LORATADINE | 
| 0363-1686 | WAL-ITIN | LORATADINE | 
| 0363-9150 | Wal-itin | Loratadine | 
| 0363-2085 | Wal-itin Allergy Relief | Loratadine |