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Sun protection body
Sun protection body - 76157-511-02 - (Avobenzone, Homosalate, Octislate, Oxybenzone)
Drug Information of Sun protection body
| Product NDC: | 76157-511 |
| Proprietary Name: | Sun protection body |
| Non Proprietary Name: | Avobenzone, Homosalate, Octislate, Oxybenzone |
| Active Ingredient(s): | 3; 7; 5 mL/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Homosalate, Octislate, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sun protection body
| Product NDC: | 76157-511 |
| Labeler Name: | La Prairie Group AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110214 |
Package Information of Sun protection body
| Package NDC: | 76157-511-02 |
| Package Description: | 1 BOTTLE in 1 BOX (76157-511-02) > 180 mL in 1 BOTTLE (76157-511-01) |
NDC Information of Sun protection body
| NDC Code | 76157-511-02 |
| Proprietary Name | Sun protection body |
| Package Description | 1 BOTTLE in 1 BOX (76157-511-02) > 180 mL in 1 BOTTLE (76157-511-01) |
| Product NDC | 76157-511 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octislate, Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110214 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | La Prairie Group AG |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE |
| Strength Number | 3; 7; 5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
