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Ole Henriksen
Ole Henriksen - 51770-001-02 - (Octinoxate, Avobenzone, Oxybenzone, Octocrylene)
Drug Information of Ole Henriksen
| Product NDC: | 51770-001 |
| Proprietary Name: | Ole Henriksen |
| Non Proprietary Name: | Octinoxate, Avobenzone, Oxybenzone, Octocrylene |
| Active Ingredient(s): | 2; 7.5; 1.9; 2 g/100g; g/100g; g/100g; g/100g & nbsp; Octinoxate, Avobenzone, Oxybenzone, Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ole Henriksen
| Product NDC: | 51770-001 |
| Labeler Name: | Ole Henriksen |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100815 |
Package Information of Ole Henriksen
| Package NDC: | 51770-001-02 |
| Package Description: | 1 JAR in 1 PACKAGE (51770-001-02) > 50 g in 1 JAR (51770-001-01) |
NDC Information of Ole Henriksen
| NDC Code | 51770-001-02 |
| Proprietary Name | Ole Henriksen |
| Package Description | 1 JAR in 1 PACKAGE (51770-001-02) > 50 g in 1 JAR (51770-001-01) |
| Product NDC | 51770-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Avobenzone, Oxybenzone, Octocrylene |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100815 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ole Henriksen |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 2; 7.5; 1.9; 2 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
