OTC - ACTIVE INGREDIENT SECTION
Active Ingredient
Benzalkonium CI 0.13%
Lidocaine 2.5%
First Aid Antiseptic Spray
- Manufacturer
- Inspec Solutions LLC.
- Effective date
- 2021-06-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:43:19
Label at a glance#
ProductDG health
Active ingredientBENZALKONIUM CHLORIDE, LIDOCAINE
Label structure10 sections
Label contents#
Full prescribing information#
OTC - WHEN USING SECTION
When using this product
do not use in or near the eye
do not apply over large areas of the body or in large quantities
do not apply over raw surface or blistered areas
OTC - PURPOSE SECTION
Benzalkonium CI 0.13% ......... First Aid Antiseptic
Lidocaine 2.5% ...................... Pain Relieving Spray
OTC - STOP USE SECTION
Stop use and ask a doctor if
condition worsens
symptoms presist for over than 7 days, or clear up and occur sgain within a few days
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
INACTIVE INGREDIENT SECTION
PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE
SODIUM PHOSPHATE DIBASIC
NONOXYNOL-9
EDETATE DISODIUM
purified Water
METHYLPARABEN
DIAZOLIDINYL UREA
PROPYLPARABEN
WARNINGS SECTION
WARNINGS
For external use only.
When using this product:
do not use in or near the eye
do not apply over large areas of the body or in large quantities
do not apply over raw surface or blistered areas
Stop use and ask a doctor if
condition worsens
symptoms presist for over than 7 days, or clear up and occur sgain within a few days
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
INDICATIONS & USAGE SECTION
Uses
first aid to help prevent bacterial contamination or skin infection, and for temporary relief of pain and itching associated with minor: cute, scrapes, burns, sunburn, skin irritations
DOSAGE & ADMINISTRATION SECTION
Directions
Spray small amount on the area 1-3 times daily
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72667-006-01 | 2023-01-30 | C162847 | 48780-1 | 9d75b9d0-c439-f424-e053-dadaa90a57ce | First Aid Antiseptic Spray |
| 72667-006-01 | 2021-06-17 | C162847 | 48780-1 | 9d75b9d0-c439-f424-e053-dadaa90a57ce | First Aid Antiseptic Spray |
| 72667-006-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-c439-f424-e053-dadaa90a57ce | First Aid Antiseptic Spray |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- DG health
- Benzalkonium, Lidocaine
- SODIUM PHOSPHATE DIBASIC DIHYDRATE
- NONOXYNOL-9
- EDETATE DISODIUM
- EDETIC ACID
- WATER
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- LIDOCAINE
- DIAZOLIDINYL UREA
- METHYLPARABEN
- PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE
- PROPYLPARABEN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72667-006 | 72667-006-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM PHOSPHATE DIBASIC DIHYDRATE | 94255I6E2T | IACT |
| NONOXYNOL-9 | 48Q180SH9T | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| WATER | 059QF0KO0R | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| LIDOCAINE | 98PI200987 | ACTIB |
| DIAZOLIDINYL UREA | H5RIZ3MPW4 | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE | O4446S9CRA | IACT |
| PROPYLPARABEN | Z8IX2SC1OH | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 49eb807b-fa33-3d84-e063-6394a90acfcf | 7cd6b829-3500-60dd-e053-2991aa0aad12 | 2026-02-03 | Warnings | 7cd6b829-3500-60dd-e053-2991aa0aad12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.