Touchland The Bright Nights Set
- Product NDC
- 10237-134
- Requested package NDC
- 10237-134-00
- 11-digit product format
- 102370134
- Labeler code
- 10237
- Product ID
- 10237-134_5b11f303-c2f7-bc44-e063-6294a90a5776
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- KIT
- Labeler
- Church & Dwight Co., Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-01
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Touchland The Bright Nights Set
- Listing expiration
- 2027-12-31
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1041849 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 5b11f0e8-5903-e723-e063-6394a90a71e6 | Available on FDA.report |
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 |
|---|---|---|---|---|---|---|
| Touchland The Bright Nights Set | ALCOHOL | Church & Dwight Co., Inc. | 5b11f0e8-5903-e723-e063-6394a90a71e6 | 2026-09-09 | Warnings | 10237-134-00 10237-134 10237013400 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 10237-134-00 | 10237013400 | 1 KIT in 1 BOX (10237-134-00) / 1 KIT in 1 KIT * 1 BOTTLE, SPRAY in 1 CASE (10237-125-00) / 30 mL in 1 BOTTLE, SPRAY * 30 mL in 1 BOTTLE, SPRAY (10237-126-00) | 1 kit | 2026-08-01 | No | No | Current |