BLEMISH
- Product NDC
- 63550-194
- 11-digit product format
- 635500194
- Labeler code
- 63550
- Product ID
- 63550-194_75dc31bc-4d3f-482d-abd3-d60cdddcf89d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Kamins Dermatologics Inc.
- Application
- part333D
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-10-19
- Marketing end
- 0000-00-00
- Substance
- BENZOYL PEROXIDE
- Active strength
- 100 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| a46239a7-5963-4008-8cbb-6b9000f497eb | Product name | 1 | 20250721 |
| b382b4e1-6b48-45f6-bffc-e61b00b0ce19 | Product name | 3 | 20250317 |
| d9d61457-6a5a-41fc-b418-e5479a2904b7 | Product name | 2 | 20230303 |
| 32012d5c-25ac-49c7-9d4c-1313177fff7c | Product name | 1 | 20230112 |
| 13e7e7e3-e885-4c79-af6d-dad1aedbb06e | Product name | 1 | 20220128 |
| 4a7d44fe-774d-404b-aad0-8a90fe78375a | Product name | 4 | 20211025 |
| 3f45980c-c196-47e5-0e5e-48b7c57327c5 | Product name | 5 | 20200428 |
| d12e2d7c-bd6b-45d4-94f9-6df8e1b8b27b | Product name | 3 | 20200203 |
| ee5c6de5-d9cd-454f-b250-7b19e5cf2992 | Product name | 4 | 20190619 |
| ad75fcfd-a339-42a1-9c60-43ba2c654cfa | Product name | 1 | 20170810 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63550-194-23 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-d3dc-f424-e053-dadaa90a57ce | BLEMISH GEL 10% CONSUMER LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63550-194-23 | BLEMISH | 30 mL in 1 BOX | GEL | 30 | 1 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BENZOYL PEROXIDE | ACTIVE INGREDIENT | W9WZN9A0GM | BLEMISH (BENZOYL PEROXIDE) GEL [KAMINS DERMATOLOGICS INC.] | 1 | |
| BENZOYL PEROXIDE | ACTIVE MOIETY | W9WZN9A0GM | BLEMISH (BENZOYL PEROXIDE) GEL [KAMINS DERMATOLOGICS INC.] | 1 | |
| ACER SACCHARUM SAP | INACTIVE INGREDIENT | 75UOH57984 | BLEMISH (BENZOYL PEROXIDE) GEL [KAMINS DERMATOLOGICS INC.] | 1 | |
| CAPRYLYL GLYCOL | INACTIVE INGREDIENT | 00YIU5438U | BLEMISH (BENZOYL PEROXIDE) GEL [KAMINS DERMATOLOGICS INC.] | 1 | |
| DIMETHICONE | INACTIVE INGREDIENT | 92RU3N3Y1O | BLEMISH (BENZOYL PEROXIDE) GEL [KAMINS DERMATOLOGICS INC.] | 1 | |
| PHENOXYETHANOL | INACTIVE INGREDIENT | HIE492ZZ3T | BLEMISH (BENZOYL PEROXIDE) GEL [KAMINS DERMATOLOGICS INC.] | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | BLEMISH (BENZOYL PEROXIDE) GEL [KAMINS DERMATOLOGICS INC.] | 1 | |
| SORBIC ACID | INACTIVE INGREDIENT | X045WJ989B | BLEMISH (BENZOYL PEROXIDE) GEL [KAMINS DERMATOLOGICS INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | BLEMISH (BENZOYL PEROXIDE) GEL [KAMINS DERMATOLOGICS INC.] | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 486131 | benzoyl peroxide 10 % Topical Gel | PSN | ffb0097e-eeca-4b89-9a11-975091255e5a | 1 |
| 486131 | benzoyl peroxide 0.1 MG/MG Topical Gel | SCD | ffb0097e-eeca-4b89-9a11-975091255e5a | 1 |
| 486131 | benzoyl peroxide 10 % Topical Gel | SY | ffb0097e-eeca-4b89-9a11-975091255e5a | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Status |
|---|---|---|---|---|
| 63550-194-23 | 63550019423 | 30 mL in 1 BOX | 30 ml | Historical |