ZITFREE

Product NDC
67234-035
11-digit product format
672340035
Labeler code
67234
Product ID
67234-035_54742c5c-0537-49fa-bf1f-6152a8cdb0a8
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOYL PEROXIDE
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Natureplex, LLC
Application
M006
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-12-01
Substance
BENZOYL PEROXIDE
Active strength
100 mg/g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ZITFREE ACNE TREATMENTBENZOYL PEROXIDENatureplex, LLC70c2e3fb-e643-467b-80fd-c40e3c3e95132026-01-29WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

Warnings For external use only. Do not use if you have very sensitive skin are sensitive to benzoyl peroxide When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time avoid unnecessary sun exposure and use a sunscreen avoid contact with the eyes, lips and mouth avoid contact with hair and dyed fabrics, which may be bleached by this product skin irritation may occur, characterized by redness, burning, itching, peeling or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration. Stop use and consult a doctor if irritation becomes severe. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away: 800-222-1222.

Additional Listing Data#

Finished product
Yes
Brand name base
ZITFREE
Brand name suffix
ACNE TREATMENT
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOYL PEROXIDE100 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiW9WZN9A0GM

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67234-035-012025-01-30C16284748780-12cef2736-8407-d83d-e063-dadaa90ab31fZITFREE ACNE TREATMENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67234-035-01ZITFREEACNE TREATMENT1 in 1 CARTONOINTMENT13
67234-035-01ZITFREEACNE TREATMENT28 g in 1 TUBEOINTMENT283

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67234-035ZITFREE ACNE TREATMENT (BENZOYL PEROXIDE) OINTMENT [NATUREPLEX LLC]2Current NDC, Legacy NDC, 2 package rows20171206_70c2e3fb-e643-467b-80fd-c40e3c3e9513.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67234-035-01672340035011 TUBE in 1 CARTON (67234-035-01) / 28 g in 1 TUBE1 tube2014-12-010000-00-00NoNoCurrent