Glytone Acne BPO Treatment Gel

Product NDC
84262-030
Requested package NDC
84262-030-01
11-digit product format
842620030
Labeler code
84262
Product ID
84262-030_4e68cba9-8359-1ee8-e063-6294a90ae4be
Type
HUMAN OTC DRUG
Nonproprietary name
Benzoyl Peroxide Gel
Dosage form
GEL
Route
TOPICAL
Labeler
Glytone, LLC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-04-02
Substance
BENZOYL PEROXIDE
Active strength
.05 g/g
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
Glytone Acne BPO Treatment Gel
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOYL PEROXIDE.05 g/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
W9WZN9A0GMInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
308694Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
4e68cba9-8358-1ee8-e063-6294a90ae4beAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a46239a7-5963-4008-8cbb-6b9000f497ebProduct name120250721
b382b4e1-6b48-45f6-bffc-e61b00b0ce19Product name320250317
d9d61457-6a5a-41fc-b418-e5479a2904b7Product name220230303
32012d5c-25ac-49c7-9d4c-1313177fff7cProduct name120230112
13e7e7e3-e885-4c79-af6d-dad1aedbb06eProduct name120220128
4a7d44fe-774d-404b-aad0-8a90fe78375aProduct name420211025
3f45980c-c196-47e5-0e5e-48b7c57327c5Product name520200428
d12e2d7c-bd6b-45d4-94f9-6df8e1b8b27bProduct name320200203
ee5c6de5-d9cd-454f-b250-7b19e5cf2992Product name420190619
ad75fcfd-a339-42a1-9c60-43ba2c654cfaProduct name120170810
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84262-030-01Glytone Acne BPO Treatment Gel60 g in 1 TUBEGEL601

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
Glytone Acne BPO Treatment GelBENZOYL PEROXIDE GELGlytone, LLC4e68cba9-8358-1ee8-e063-6294a90ae4be2026-04-02WarningsExact identifier
ndc (package): 84262-030-01
ndc (product): 84262-030
ndc11 (package): 84262003001

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308694benzoyl peroxide 5 % Topical GelPSN4e68cba9-8358-1ee8-e063-6294a90ae4be1
308694benzoyl peroxide 0.05 MG/MG Topical GelSCD4e68cba9-8358-1ee8-e063-6294a90ae4be1
308694benzoyl peroxide 5 % Topical GelSY4e68cba9-8358-1ee8-e063-6294a90ae4be1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84262-030-018426200300160 g in 1 TUBE (84262-030-01) 60 g2026-04-02NoNoCurrent