NDC 30142-458

All Day Allergy

Cetirizine Hydrochloride

All Day Allergy is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Kroger Company. The primary component is Cetirizine Hydrochloride.

Product ID30142-458_78f6be1d-ac3c-4384-b7bf-0760ddb74f15
NDC30142-458
Product TypeHuman Otc Drug
Proprietary NameAll Day Allergy
Generic NameCetirizine Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2008-01-08
Marketing CategoryANDA / ANDA
Application NumberANDA078336
Labeler NameKroger Company
Substance NameCETIRIZINE HYDROCHLORIDE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 30142-458-06

1 BOTTLE in 1 CARTON (30142-458-06) > 70 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2017-10-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 30142-458-95 [30142045895]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-09-24
Marketing End Date2019-08-01

NDC 30142-458-72 [30142045872]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-09-02
Marketing End Date2019-05-08

NDC 30142-458-06 [30142045806]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-10-02

NDC 30142-458-49 [30142045849]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-04-03

NDC 30142-458-92 [30142045892]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-15

NDC 30142-458-76 [30142045876]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-09-02
Marketing End Date2019-06-01

NDC 30142-458-88 [30142045888]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-19

NDC 30142-458-66 [30142045866]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-01-08

NDC 30142-458-39 [30142045839]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-09-13

NDC 30142-458-48 [30142045848]

All Day Allergy TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-08-10
Marketing End Date2019-05-19

Drug Details

Active Ingredients

IngredientStrength
CETIRIZINE HYDROCHLORIDE10 mg/1

OpenFDA Data

SPL SET ID:d548cf8d-e9e9-4201-89de-c5039b70414b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1014678

    • NDC Crossover Matching brand name "All Day Allergy" or generic name "Cetirizine Hydrochloride"

    NDCBrand NameGeneric Name
    70677-0006all day allergyall day allergy
    30142-458All Day AllergyAll Day Allergy
    30142-211All Day AllergyAll Day Allergy
    30142-884All Day AllergyAll Day Allergy
    36800-211All Day AllergyAll Day Allergy
    36800-741All Day AllergyAll Day Allergy
    37205-819All Day AllergyAll Day Allergy
    37808-211All Day AllergyAll Day Allergy
    41163-219all day allergyall day allergy
    41520-211All Day AllergyAll Day Allergy
    42507-211All Day AllergyAll Day Allergy
    46122-101All Day AllergyAll Day Allergy
    53187-220All Day AllergyAll Day Allergy
    53187-129All Day AllergyAll Day Allergy
    55315-211All Day AllergyAll Day Allergy
    59726-211All Day AllergyAll Day Allergy
    62011-0313all day allergyall day allergy
    62011-0552All Day AllergyAll Day Allergy
    63868-139All Day AllergyAll Day Allergy
    59726-739All Day AllergyAll Day Allergy
    62011-0408All Day AllergyAll Day Allergy
    0363-4101allergy reliefCetirizine Hydrochloride
    0113-7002Basic Care All Day AllergyCetirizine Hydrochloride
    0113-7036BASIC CARE ALL DAY ALLERGYCetirizine hydrochloride
    0121-4780Cetirizine HydrochlorideCetirizine Hydrochloride
    0179-8301Cetirizine HydrochlorideCetirizine Hydrochloride
    0179-8302Cetirizine HydrochlorideCetirizine Hydrochloride
    0363-0471Cetirizine HydrochlorideCetirizine Hydrochloride
    0363-9899Cetirizine HydrochlorideCetirizine Hydrochloride
    0378-3635Cetirizine Hydrochloridecetirizine hydrochloride
    0363-0068Cetirizine Hydrochloride (Allergy)Cetirizine Hydrochloride
    0363-9602Cetirizine Hydrochloride (Allergy)Cetirizine Hydrochloride
    0363-3311childrens allergy reliefCetirizine Hydrochloride
    0363-3393childrens allergy reliefCetirizine Hydrochloride
    0363-4025Childrens Cetirizine HydrochlorideCetirizine Hydrochloride
    0363-1884childrens dye free wal zyrcetirizine Hydrochloride
    0363-0595Childrens Wal Zyr 24 Hour Allergycetirizine Hydrochloride
    0363-0974Childrens Wal Zyr Allergycetirizine hydrochloride
    0363-1974dye free wal zyrcetirizine hydrochloride
    0113-0981Good Sense All Day Allergycetirizine hydrochloride
    0113-1036good sense all day allergyCetirizine hydrochloride
    0113-9458Good Sense all day allergyCetirizine Hydrochloride
    0363-0276wal zyrCetirizine Hydrochloride
    0363-0495Wal ZyrCetirizine Hydrochloride
    0363-2088Wal-ZyrCetirizine Hydrochloride
    0363-2102Wal-ZyrCetirizine Hydrochloride
    0363-2106Wal-ZyrCetirizine Hydrochloride
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.