FDA.reportPublic FDA data

NDC 58602-024-16 - AuroZzil NIGHTTIME SLEEP-AID

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
58602-024
Requested NDC
58602-024-16
Package NDCs from labels
58602-024-16, 58602-024-31, 58602-024-18
Manufacturer
Aurohealth LLC
Effective date
2020-11-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
AuroZzil NIGHTTIME SLEEP-AID - Aurohealth LLCAurohealth LLC2020-11-13Human OTC Drug Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DIPHENHYDRAMINE HYDROCHLORIDEACTIVE INGREDIENTTC2D6JAD40AUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
DIPHENHYDRAMINEACTIVE MOIETY8GTS82S83MAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
BERRYINACTIVE INGREDIENTFV3431923ZAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOAAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
HIGH FRUCTOSE CORN SYRUPINACTIVE INGREDIENTXY6UN3QB6SAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
POLYOXYL 40 STEARATEINACTIVE INGREDIENT13A4J4NH9IAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3AUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
SACCHARIN SODIUMINACTIVE INGREDIENTSB8ZUX40TYAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
TRISODIUM CITRATE DIHYDRATEINACTIVE INGREDIENTB22547B95KAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1
WATERINACTIVE INGREDIENT059QF0KO0RAUROZZIL NIGHTTIME SLEEP-AID (DIPHENHYDRAMINE HYDROCHLORIDE) SOLUTION [AUROHEALTH LLC]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 151 of 206 · 4,108 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bacti-GoneBACTI-GONEBeta Technology,Incbe4c1c52-c03a-5bd8-e053-2995a90a4cc72024-12-06WarningsExact identifier
unii: 3K9958V90M
Contact Instant Antiseptic Hand SanitizerCONTACT INSTANT ANTISEPTIC HAND SANITIZERUnited Laboratories, Inc.eedb3eb2-6224-f26d-e053-2995a90aec7d2024-12-06WarningsExact identifier
unii: 3K9958V90M
Alco-SanALCO-SANMid-American Research Chemical Corp.ba2306ff-d66c-fe4b-e053-2995a90a05f72024-12-06WarningsExact identifier
unii: 3K9958V90M
Instant Hand Sanitizer KE-53SANINSTANT HAND SANITIZER KE-53SANKinzua Environmentald9a829a7-851a-3811-e053-2a95a90a2b902024-12-06WarningsExact identifier
unii: 3K9958V90M
BLUESEA DISPOSABLE HAND SANITIZERALCOHOLBLUE SEA AEROSOL & DAILY CARE CO., LTD7a552be2-a9e1-4c6f-b1c2-79113a73bd2f2024-12-06WarningsExact identifier
unii: 3K9958V90M
BLUESEA INSTANT HAND SANITIZERALCOHOLBLUE SEA AEROSOL & DAILY CARE CO., LTDe6b5ce49-d6d6-4b24-8b40-bfb1fb7005bd2024-12-06WarningsExact identifier
unii: 3K9958V90M
Somnapure Clinical StrengthDIPHENHYDRAMINE HYDROCHLORIDEForce Factor Brands LLC063517c0-bcb1-46dd-85f1-bbb2f24274ef2024-12-06WarningsExact identifier
unii: TC2D6JAD40
Instant Hand AntisepticALCOHOLASP Globalb84075db-be0c-4265-b262-825bc6ade9d82024-12-06WarningsExact identifier
unii: 3K9958V90M
Instant Hand AntisepticALCOHOLASP Global9aca3f89-cdde-430c-8eb6-43a3ac3fc0df2024-12-06WarningsExact identifier
unii: 3K9958V90M
PURELL Advanced Hand Sanitizer Energizing MintALCOHOLGOJO Industries, Inc.a77f2ac3-2a8c-45e7-a65e-bd58e834249b2024-12-05WarningsExact identifier
unii: 3K9958V90M
InstantINSTANTUnlimited Salesbd310bb2-37e5-1ed7-e053-2995a90a36b42024-12-05WarningsExact identifier
unii: 3K9958V90M
ALPET E3 PLUS HAND SANITIZERALCOHOLBest Sanitizers, Inc.d6d64945-4cd4-4926-9ef9-898cea89e8112024-12-05WarningsExact identifier
unii: 3K9958V90M
SMART SAN HAND SANITIZERALCOHOLBest Sanitizers, Inc.1c018851-82e0-4f2c-8f40-31674cd6fe2b2024-12-05WarningsExact identifier
unii: 3K9958V90M
ALPET E3 HAND SANITIZER FOAMALCOHOLBest Sanitizers, Inc.53573e1a-a3f8-4598-8248-ec4a62392d002024-12-05WarningsExact identifier
unii: 3K9958V90M
SMART SAN HAND SANITIZER FRAGRANCE-FREEALCOHOLBest Sanitizers, Inc.bce412dc-21db-4c63-b4fc-33538cda74242024-12-05WarningsExact identifier
unii: 3K9958V90M
SMART SAN HAND SANITIZERALCOHOLBest Sanitizers, Inc.8a2cc051-604c-43a7-9f65-2f929b759daa2024-12-05WarningsExact identifier
unii: 3K9958V90M
OPS 70 PERCENT ALCOHOL FOAMING SKIN SANITIZERETHYL ALCOHOLArcher Manufacturing, Inc.d05fbe85-26de-0d24-e053-2a95a90ab5cb2024-12-05WarningsExact identifier
unii: 3K9958V90M
BLACK OPS 70 PERCENT ALCOHOL FOAMING SKIN SANITIZERETHYL ALCOHOLArcher Manufacturing, Inc.d334b7f0-01dc-7f59-e053-2a95a90a06b52024-12-05WarningsExact identifier
unii: 3K9958V90M
alcohol pad 01ALCOHOLCosmuses Cosmetics (Ningbo) Co., Ltd.03a6e8d4-535d-b316-e063-6294a90aebf52024-12-04WarningsExact identifier
unii: 3K9958V90M
Watermelon Hand Sanitizer Spray. 01ALCOHOLShenzhen Lantern Scicence Co.,Ltd.1f0f9885-2ad5-09de-e063-6394a90ad0d72024-12-03WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.