Product NDC: | 0299-3913 |
Proprietary Name: | Cetaphil DermaControl SPF 30 |
Non Proprietary Name: | octocrylene, octisalate, avobenzone |
Active Ingredient(s): | 3; 5; 7 mL/100mL; mL/100mL; mL/100mL & nbsp; octocrylene, octisalate, avobenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0299-3913 |
Labeler Name: | Galderma Laboratories, L.P. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111201 |
Package NDC: | 0299-3913-04 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (0299-3913-04) > 118 mL in 1 BOTTLE, PUMP |
NDC Code | 0299-3913-04 |
Proprietary Name | Cetaphil DermaControl SPF 30 |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (0299-3913-04) > 118 mL in 1 BOTTLE, PUMP |
Product NDC | 0299-3913 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | octocrylene, octisalate, avobenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20111201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Galderma Laboratories, L.P. |
Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE |
Strength Number | 3; 5; 7 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |