Escudo Ultra-Protect Original
- Manufacturer
- Indelpa, Inc
- Effective date
- 2026-02-03
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 01:36:26
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active Ingredient
Active Ingredient ------------------------------- Purpose
Benzalkonium Chloride 0.1% ----------------- Antibacterial
OTC - PURPOSE SECTION
Active Ingredient ------------------------------- Purpose
Benzalkonium Chloride 0.1% ----------------- Antibacterial
Use
for washing to decrease becateria on the skin.
Warnings
For external use only.
Do not use if
you are allergic to any of the ingredients
Directions
- Wet bar with water.
- Lather vigorously and wash skin.
- Rinse with water and dry thoroughly.
When using this product
avoid contact with eyes. In case of eye contact, rinse thoroughly with water.
Stop use and ask a doctor if
irritation or redness develop and persist for more than 72 hours.
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredients
Alcohol, D&C Red 33, Etidronic Acid, FD&C Green 3, Glycerin, Sodium Chloride, Sodium Palmate, Sodium Palm Kernelate, Tetrasodium EDTA, Titanium Dioxide, Water, Fragance.
Questions or Comments?
1-800-678-5082 info@indelpa.com.mx
SPL UNCLASSIFIED SECTION
*effective only against E. coli and S. Aureus.
Distributed by Indelpa, Inc.
18911 Hardy Oak Blvd Suite 327
San Antonio, TX 78258.
MADE IN COLOMBIA
Package Label principal display panel
Eliminates 99.9%
of Bacteria
Fresh clean scent
Deep cleansing
Escudo®
ULTRA-PROTECT
ORIGINAL
ANTIBACTERIAL BAR SOAP
NET WT 4.05 Z (115g)
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84529-001-01 | Escudo Ultra-Protect Original | 115 g in 1 CELLO PACK | SOAP | 115 | 3 |
Products#
Every source-derived product name is available through these pages.
- Escudo Ultra-Protect Original
- Benzalkonium Chloride
- WATER
- ETIDRONIC ACID
- GLYCERIN
- BENZALKONIUM
- FD&C GREEN NO. 3
- EDETATE SODIUM
- D&C RED NO. 33
- FRAGRANCE 13576
- SODIUM PALMATE
- SODIUM CHLORIDE
- TITANIUM DIOXIDE
- ALCOHOL
- SODIUM PALM KERNELATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84529-001 | 84529-001-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ETIDRONIC ACID | M2F465ROXU | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| FD&C GREEN NO. 3 | 3P3ONR6O1S | IACT |
| EDETATE SODIUM | MP1J8420LU | IACT |
| D&C RED NO. 33 | 9DBA0SBB0L | IACT |
| FRAGRANCE 13576 | 5EM498GW35 | IACT |
| SODIUM PALMATE | S0A6004K3Z | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| SODIUM PALM KERNELATE | 6H91L1NXTW | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 2 | 2025-12-31 | monthly-update | 2026-06-03 17:51:05 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Escudo Ultra-Protect Original | BENZALKONIUM CHLORIDE | Indelpa, Inc | 1cd4c38f-8156-bd74-e063-6394a90a9f56 | 2026-02-03 | Warnings | 84529-001-01 84529-001 84529000101 49f146b4-8bdf-2df2-e063-6294a90a95f6 1cd4c38f-8156-bd74-e063-6394a90a9f56 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
