NDC 51596-009

Allergy Attack Relief to Go

Diphenhydramine Hydrochloride

Allergy Attack Relief to Go is a Oral Powder in the Human Otc Drug category. It is labeled and distributed by Breakthrough Products Inc.. The primary component is Diphenhydramine Hydrochloride.

• Product ID: 51596-009_8ffb4f55-f838-4a59-8894-158acb12af74
• NDC: 51596-009
• Product Type: Human Otc Drug
• Proprietary Name: Allergy Attack Relief to Go
• Generic Name: Diphenhydramine Hydrochloride
• Dosage Form: Powder
• Route of Administration: ORAL
• Marketing Start Date: 2012-10-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Breakthrough Products Inc.
• Substance Name: DIPHENHYDRAMINE HYDROCHLORIDE
• Active Ingredient Strength: 25 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51596-009-01

1 POWDER in 1 POUCH (51596-009-01)

• Marketing Start Date: 2012-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51596-009-12 [51596000912]

Allergy Attack Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-01
• Inactivation Date: 2020-01-31

NDC 51596-009-05 [51596000905]

Allergy Attack Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-01
• Inactivation Date: 2020-01-31

NDC 51596-009-10 [51596000910]

Allergy Attack Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-10-16
• Inactivation Date: 2020-01-31

NDC 51596-009-24 [51596000924]

Allergy Attack Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-01
• Inactivation Date: 2020-01-31

NDC 51596-009-01 [51596000901]

Allergy Attack Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
DIPHENHYDRAMINE HYDROCHLORIDE	25 mg/1

OpenFDA Data

• SPL SET ID: 2da1341d-5c2d-47ef-8498-f58fbb4f6300
• Manufacturer:
  • Breakthrough Products Inc.
• UNII:
  • TC2D6JAD40
• RxNorm Concept Unique ID - RxCUI:
  • 1312784

NDC Crossover Matching brand name "Allergy Attack Relief to Go" or generic name "Diphenhydramine Hydrochloride"

NDC	Brand Name	Generic Name
51596-009	Allergy Attack Relief to Go	Allergy Attack Relief to Go
0363-7100	Adult Allergy Relief	Diphenhydramine Hydrochloride
0363-0100	ALLERGY RELIEF	DIPHENHYDRAMINE HYDROCHLORIDE
0113-7479	basic care allergy relief	Diphenhydramine Hydrochloride
0363-0710	childrens Allergy Dye Free Wal Dryl	Diphenhydramine hydrochloride
0363-0004	Childrens WAL-DRYL	Diphenhydramine Hydrochloride
0121-0865	Diphenhydramine HCl Oral Solution	diphenhydramine hydrochloride
0121-1730	Diphenhydramine HCl Oral Solution	diphenhydramine hydrochloride
0121-0489	DIPHENHYDRAMINE HYDROCHLORIDE	DIPHENHYDRAMINE HYDROCHLORIDE
0121-0978	DIPHENHYDRAMINE HYDROCHLORIDE	DIPHENHYDRAMINE HYDROCHLORIDE
0185-0648	diphenhydramine hydrochloride	diphenhydramine hydrochloride
0185-0649	diphenhydramine hydrochloride	diphenhydramine hydrochloride
0363-0293	Dye Free Wal Dryl Allergy	Diphenhydramine Hydrochloride
0363-0753	Dye Free Wal Sleep Z	DIPHENHYDRAMINE HYDROCHLORIDE
0113-0462	Good Sense Allergy Relief	diphenhydramine hydrochloride
0113-0479	good sense allergy relief	Diphenhydramine Hydrochloride
0113-0431	good sense nighttime sleep aid	Diphenhydramine Hydrochloride
0113-1909	good sense sleep aid	diphenhydramine hydrochloride
0363-0092	Wal Dryl	Diphenhydramine Hydrochloride
0363-0379	wal dryl allergy	Diphenhydramine Hydrochloride
0363-0060	Wal-Sleep Z	Diphenhydramine Hydrochloride
0363-0223	Wal-Som	Diphenhydramine hydrochloride