Viabecline First Aid Antibiotic

Manufacturer
VIADERMA II, INC.
Effective date
2023-11-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:19:32

Label at a glance#

ProductViabecline First Aid Antibiotic
Active ingredientTETRACYCLINE HYDROCHLORIDE
Label structure7 sections

Dosage and administration

Clean the affected area. Apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily. May be covered with a sterile bandage.

Label contents#

Full prescribing information#

Active ingredient (in each gram)

OTC - ACTIVE INGREDIENT SECTION

Tetracycline hydrochloride 30 mg

Purpose

OTC - PURPOSE SECTION

First Aid Antibiotic

Use

INDICATIONS & USAGE SECTION

First aid to help prevent skin infection in minor cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For external use only. May be harmful if swallowed.

Do not use if allergic to any ingredient listed on this label. Allergy alert:

Do not use 

OTC - DO NOT USE SECTION

  • in the eyes
  • over large areas of the body 
  • longer than 1 week unless directed by doctor

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds 
  • animal bites
  • serious burns

Stop use and ask a doctor 

OTC - STOP USE SECTION

if condition persists or gets worse.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean the affected area.
  • Apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily.
  • May be covered with a sterile bandage.

Other information

SPL UNCLASSIFIED SECTION

  • Keep product refrigerated to pressrve its effectiveness and color
  • Stop use if product is misused: If the bottle is left open and/or if not refrigerated, the liquid will tend to turn black over time. Discard the product if the liquid turns black due to misuse.
  • This product is an OTC antibiotic for human use.
  • Containa no alcohol,no animal ingredients.
  • Blended for typical skin color.
  • May stain cloth.
  • No claims regarding stem cell healing are implied for this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

ACETIC ACID, ASCORBIC ACID, CHLORHEXIDINE GLUCONATE, CHOLECALCIFEROL, DIMETHYL SULFOXIDE, DIPROPYLENE GLYCOL, GLUCONO DELTA LACTONE, GLYCERIN, HISTIDINE, HYDROXETHYL CELLULOSE, MAGNESIUM STEARATE, METHYLPARABEN, SODIUM HYDROXIDE, SORBIC ACID, STEARIC ACID, WATER

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69006-00569006-005-00, 69006-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Source Document#

Source XML · Source PDF

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
29a68276-86ef-b068-e063-6294a90ad3498ce60b99-ac83-4bb2-8de9-e4115bd5667c2024-12-19WarningsExact identifier
spl set id: 8ce60b99-ac83-4bb2-8de9-e4115bd5667c

Reported adverse events (FAERS/openFDA)#

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