Banophen is a Oral Capsule in the Human Otc Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Diphenhydramine Hydrochloride.
Product ID | 71335-0081_098951c1-7358-484f-bc3b-6629470ee8e2 |
NDC | 71335-0081 |
Product Type | Human Otc Drug |
Proprietary Name | Banophen |
Generic Name | Diphenhydramine Hcl |
Dosage Form | Capsule |
Route of Administration | ORAL |
Marketing Start Date | 2009-11-02 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part348 |
Labeler Name | Bryant Ranch Prepack |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Active Ingredient Strength | 50 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2022-02-09 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-11-03 |
Ingredient | Strength |
---|---|
DIPHENHYDRAMINE HYDROCHLORIDE | 50 mg/1 |
SPL SET ID: | 20f00537-2c8a-45d1-8e5f-ec276d0a47b6 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
68071-3353 | banophen | banophen |
68151-2908 | Banophen | Banophen |
70518-0285 | Banophen | Banophen |
70518-1442 | Banophen | Banophen |
70518-1289 | Banophen | Banophen |
71335-0081 | Banophen | Banophen |
0904-5354 | Banophen | Banophen |
0904-5174 | Banophen | Banophen |
0904-1228 | banophen | banophen |
0904-2035 | Banophen | Banophen |
0904-5307 | Banophen | Banophen |
0904-5551 | Banophen | Banophen |
17856-5174 | Banophen | Banophen |
50090-2935 | banophen | banophen |
50436-3762 | Banophen | Banophen |
55700-678 | Banophen | Banophen |
63187-315 | banophen | banophen |
68788-7830 | Banophen | Banophen |
0113-7379 | basic care childrens allergy relief | Diphenhydramine HCl |
0113-7186 | basic care nighttime sleep aid | Diphenhydramine HCl |
0113-7506 | basic care nighttime sleep aid | diphenhydramine hcl |
0363-0481 | Childrens Allergy Dye-Free Wal Dryl | Diphenhydramine HCl |
0113-0379 | good sense allergy | Diphenhydramine HCl |
0113-0052 | good sense sleep time | Diphenhydramine HCl |
0113-0186 | Good Sense Sleep Time | Diphenhydramine HCl |
0363-0353 | Itch Relief Gel | Diphenhydramine HCl |
0363-0236 | Nighttime Sleep Aid | Diphenhydramine HCl |
0363-0367 | Sleep Aid | Diphenhydramine HCl |
0363-0189 | Sleep II | Diphenhydramine HCl |
0363-0190 | Wal-Dryl | Diphenhydramine HCl |
0363-0418 | Wal-Dryl | Diphenhydramine HCl |
0363-0329 | WAL-DRYL ALLERGY | Diphenhydramine HCl |
0363-0020 | Wal-Sleep Z | Diphenhydramine HCl |