Allegra Allergy, Travel BASIX
- Product NDC
- 66715-6507
- 11-digit product format
- 667156507
- Labeler code
- 66715
- Product ID
- 66715-6507_5076f5eb-2ebc-5623-e063-6394a90a3fff
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lil' Drug Store Products, Inc
- Application
- NDA020872
- Marketing category
- NDA
- Marketing start
- 2022-10-11
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Allegra Allergy, Travel BASIX
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FEXOFENADINE HYDROCHLORIDE | 180 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2S068B75ZU |
| Rxcui | 997420, 997422 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66715-6507-2 | Allegra Allergy, Travel BASIX | 2 in 1 CARTON | TABLET, FILM COATED | 2 | | 9 |
| 66715-6507-2 | Allegra Allergy, Travel BASIX | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 9 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| Fexofenadine Hydrochloride | ACTIVE INGREDIENT | 2S068B75ZU | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
| FEXOFENADINE | ACTIVE MOIETY | E6582LOH6V | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
| Cellulose, Microcrystalline | INACTIVE INGREDIENT | OP1R32D61U | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
| Croscarmellose Sodium | INACTIVE INGREDIENT | M28OL1HH48 | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
| Hypromelloses | INACTIVE INGREDIENT | 3NXW29V3WO | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
| Magnesium Stearate | INACTIVE INGREDIENT | 70097M6I30 | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
| Polyethylene Glycols | INACTIVE INGREDIENT | 3WJQ0SDW1A | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
| Silicon Dioxide | INACTIVE INGREDIENT | ETJ7Z6XBU4 | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
| Titanium Dioxide | INACTIVE INGREDIENT | 15FIX9V2JP | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [LIL' DRUG STORE PRODUCTS, INC] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66715-6507 | ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET, FILM COATED ALLEGRA ALLERGY, TRAVEL BASIX (FEXOFENADINE HYDROCHLORIDE) TABLET, FILM COATED [LIL' DRUG STORE PRODUCTS, INC] | 8 | Current NDC, 2 package rows | 20241121_b82d993a-16ff-4037-a182-7010de8e1cdd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 66715-6507-2 | 66715650702 | 2 BLISTER PACK in 1 CARTON (66715-6507-2) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 2022-10-11 | No | No | Current |