Lightning X Antiseptic
- Manufacturer
- Nantong Health & Beyond Hygienic Products Inc.
- Effective date
- 2024-01-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:06:50
Label at a glance#
ProductLightning X Antiseptic
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections
Label contents#
Full prescribing information#
WARNINGS SECTION
INACTIVE INGREDIENT SECTION
INDICATIONS & USAGE SECTION
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
OTC - PURPOSE SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 7792dadb-52b6-46b6-8fdf-80b1171065b5 | Product name | 1 | 20180810 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43473-303-01 | Lightning X Antiseptic | 59.1 mL in 1 BOTTLE | SPRAY | 59.1 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Lightning X Antiseptic
- Benzalkonium Chloride
- WATER
- BENZALKONIUM
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43473-303 | 43473-303-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| ALCOHOL | 3K9958V90M | 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 |
|---|---|---|---|---|---|---|
| Lightning X Antiseptic | BENZALKONIUM CHLORIDE | Nantong Health & Beyond Hygienic Products Inc. | 0e6b10e7-6e84-6bfc-e063-6294a90a8537 | 2024-01-08 | Warnings | 43473-303-01 43473-303 43473030301 0e6b10e7-6e85-6bfc-e063-6294a90a8537 0e6b10e7-6e84-6bfc-e063-6294a90a8537 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
