Savannah

Manufacturer
Med-Nap LLC
Effective date
2016-06-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:25:33

Label at a glance#

ProductSavannah Antiseptic
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

Tear open packet, unfold and use as a washcloth.

Label contents#

Full prescribing information#

Drug FactsActive Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.133%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use

INDICATIONS & USAGE SECTION

Antiseptic cleansing of face, hands and body without soap and water. Air dries in seconds.

Warnings

WARNINGS SECTION

For external use only. Do not use around eyes.

Stop use if

OTC - STOP USE SECTION

if irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Caution Keep Out of Reach of Children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open packet, unfold and use as a washcloth.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Kathon CG, Water

Savannah product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Savannah

NDC 59647-749-02

Antiseptic Towelette

Contains Benzalkoniun Chloride

For External use Only

1 Towelette

R & R Enterprises

(800) 955-2259

Made in USA

EXP: 07/18

LOT 20016 ABC

Med-Nap Savannah labelMed-Nap Savannah label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59647-749-022021-07-23C16284748780-1c7ccaba7-2427-fd44-e053-dadaa90aa01bSavannah - 749

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59647-749SAVANNAH ANTISEPTIC (BENZALKONIUM CHLORIDE) LIQUID [MED-NAP LLC]1Legacy NDC20160701_aeb379c3-dff1-4ebf-9b3e-7800860097da.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59647-74959647-749-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a55a0453-d5ce-4d13-95d5-92ac11258e38aeb379c3-dff1-4ebf-9b3e-7800860097da2016-06-30WarningsExact identifier
spl id: a55a0453-d5ce-4d13-95d5-92ac11258e38
spl set id: aeb379c3-dff1-4ebf-9b3e-7800860097da

Reported adverse events (FAERS/openFDA)#

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