Product NDC: | 23667-000 |
Proprietary Name: | Hawaiian Tropic Baby |
Non Proprietary Name: | OCTOCRYLENE, OXYBENZONE |
Active Ingredient(s): | 8; 3.5 mL/100mL; mL/100mL & nbsp; OCTOCRYLENE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 23667-000 |
Labeler Name: | Formulated Solutions |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100726 |
Package NDC: | 23667-000-01 |
Package Description: | 177 mL in 1 BOTTLE (23667-000-01) |
NDC Code | 23667-000-01 |
Proprietary Name | Hawaiian Tropic Baby |
Package Description | 177 mL in 1 BOTTLE (23667-000-01) |
Product NDC | 23667-000 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTOCRYLENE, OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100726 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Formulated Solutions |
Substance Name | OCTOCRYLENE; OXYBENZONE |
Strength Number | 8; 3.5 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |