all day Allergy Relief D
- Product NDC
- 37808-176
- 11-digit product format
- 378080176
- Labeler code
- 37808
- Product ID
- 37808-176_59443634-77c7-4cec-a287-c44187e1063e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl, Pseudoephedrine HCl
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA077170
- Marketing category
- ANDA
- Marketing start
- 2008-05-02
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| CETIRIZINE HYDROCHLORIDE | ACTIVE INGREDIENT | 64O047KTOA | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| PSEUDOEPHEDRINE HYDROCHLORIDE | ACTIVE INGREDIENT | 6V9V2RYJ8N | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| CETIRIZINE | ACTIVE MOIETY | YO7261ME24 | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| PSEUDOEPHEDRINE | ACTIVE MOIETY | 7CUC9DDI9F | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| HYDROXYPROPYL CELLULOSE (TYPE H) | INACTIVE INGREDIENT | RFW2ET671P | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-176 | ALL DAY ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B] | 4 | Legacy NDC | 20181207_a00190fc-ca0f-411e-93e9-228baec5088f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-176-53 | 37808017653 | 2 BLISTER PACK in 1 CARTON (37808-176-53) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2008-05-02 | 0000-00-00 | No | No | Current |
| 37808-176-62 | 37808017662 | 4 BLISTER PACK in 1 CARTON (37808-176-62) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 4 blister pack | 2012-07-03 | 0000-00-00 | No | No | Current |