Touchland The Bright Nights Set

Product NDC
10237-134
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#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1041849Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5b11f0e8-5903-e723-e063-6394a90a71e6Available 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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Touchland The Bright Nights SetALCOHOLChurch & Dwight Co., Inc.5b11f0e8-5903-e723-e063-6394a90a71e62026-09-09WarningsExact identifier
ndc (product): 10237-134

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
10237-134-00102370134001 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 kit2026-08-01NoNoCurrent