Product NDC: | 66382-222 |
Proprietary Name: | La Roche-Posay Laboratoire Dermatologique Anthelios 45 |
Non Proprietary Name: | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
Active Ingredient(s): | 1.5; 5; 2.5; 2.5; 3 mL/50mL; mL/50mL; mL/50mL; mL/50mL; mL/50mL & nbsp; Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66382-222 |
Labeler Name: | Laboratoires Industriels de Vichy (LIDV) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100401 |
Package NDC: | 66382-222-01 |
Package Description: | 1 BOTTLE in 1 CARTON (66382-222-01) > 50 mL in 1 BOTTLE |
NDC Code | 66382-222-01 |
Proprietary Name | La Roche-Posay Laboratoire Dermatologique Anthelios 45 |
Package Description | 1 BOTTLE in 1 CARTON (66382-222-01) > 50 mL in 1 BOTTLE |
Product NDC | 66382-222 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone Homosalate Octisalate Octocrylene Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100401 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Laboratoires Industriels de Vichy (LIDV) |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 1.5; 5; 2.5; 2.5; 3 |
Strength Unit | mL/50mL; mL/50mL; mL/50mL; mL/50mL; mL/50mL |
Pharmaceutical Classes |