Geri Dryl

Manufacturer
VERITYRX, LLC
Effective date
2025-11-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:20:31

Label at a glance#

ProductGeri Dryl
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each 5 mL teaspoonful)

Diphenhydramine HCl 12.5 mg

OTC - PURPOSE SECTION

Purpose

Antihistamine

INDICATIONS & USAGE SECTION

Uses

  • Temporarily relieves these symptoms of hay fever or other upper respiratory allergies:
  • runny nose
  • itchy nose or throat
  • sneezing
  • itchy, watery eyes
  • Temporarily relieves these symptoms due to the common cold:
  • runny nose
  • sneezing

WARNINGS SECTION

Warnings

Do not use

  • with any other product conatining diphenhydramine, including one used on the skin
  • to make a child sleepy

Ask a doctor before use if you have

  • a breathing problem such as chronic bronchitis or emphysema
  • trouble urinating due to enlarged prostate gland
  • glaucoma

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

  • excitability may occur, especially in children
  • marked drowsiness may occur
  • be careful when driving motor vehicle or operating machinery
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • do not exceed recommended dose
  • take every 4 to 6 hours as needed, or as directed by a doctor
  • do not take more than 6 doses in 24 hours
  • adults and children 12 years and over: 10 to 20 mL (2 to 4 teaspoonful)
  • children under 12 years: consult a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients: Artificial and natural cherry flavor, citric acid, FD&C #40, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate, sucralose and sucrose.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

diphenhydraminediphenhydramine

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049906diphenhydrAMINE HCl 12.5 MG in 5 mL Oral SolutionPSN1
1049906diphenhydramine hydrochloride 2.5 MG/ML Oral SolutionSCD1
1049906diphenhydramine HCl 12.5 MG per 5 ML Oral SolutionSY1
1049906diphenhydramine hydrochloride 25 MG per 10 ML Oral SolutionSY1
1049906diphenhydramine hydrochloride 50 MG per 20 ML Oral SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIPHENHYDRAMINE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeData Matrix(01)00383939000731(21)02495101(10)024951(17)260401GTIN-14: 00383939000731
GTIN-12: 383939000731
UPC-A: 383939000731
EAN-13: 0383939000731
GTIN storage (14 digits): 00383939000731
Diphenhydramine 000703 (002).jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83939-0007-1Geri Dryl5 mL in 1 CUP, UNIT-DOSELIQUID51
83939-0007-2Geri Dryl10 in 1 BOX, UNIT-DOSELIQUID101
83939-0007-2Geri Dryl5 mL in 1 CUP, UNIT-DOSELIQUID51
83939-0007-3Geri Dryl5 mL in 1 CUP, UNIT-DOSELIQUID51
83939-0007-3Geri Dryl40 in 1 BOX, UNIT-DOSELIQUID401
83939-0007-4Geri Dryl50 in 1 BOX, UNIT-DOSELIQUID501
83939-0007-4Geri Dryl5 mL in 1 CUP, UNIT-DOSELIQUID51
83939-0007-5Geri Dryl5 mL in 1 CUP, UNIT-DOSELIQUID51
83939-0007-5Geri Dryl100 in 1 BOX, UNIT-DOSELIQUID1001

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
57896-980-16ML - Milliliter57896-980526254d0-b30e-4761-bac9-2d7a454e684a12019-12-10

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83939-000783939-0007-1, 83939-0007-2, 83939-0007-3, 83939-0007-4, 83939-0007-5
57896-980

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

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 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Geri DrylDIPHENHYDRAMINE HCLVERITYRX, LLC42a05f69-0599-5571-e063-6394a90a37d32025-11-02WarningsExact identifier
ndc (package): 83939-0007-2
ndc (package): 83939-0007-4
ndc (package): 83939-0007-5
ndc (package): 83939-0007-1
ndc (package): 83939-0007-3
ndc (product): 83939-0007
ndc11 (package): 83939000705
ndc11 (package): 83939000701
ndc11 (package): 83939000703
ndc11 (package): 83939000702
ndc11 (package): 83939000704
spl id: 42a051de-5e9b-e0b7-e063-6294a90aaaa2
spl set id: 42a05f69-0599-5571-e063-6394a90a37d3
Geri DrylDIPHENHYDRAMINE HCLGERI-CARE PHARMACEUTICALS, CORP34d36146-6827-4800-8483-c0edb8f4cc282024-12-23WarningsExact identifier
ndc (product): 57896-980

Reported adverse events (FAERS/openFDA)#

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