| Product NDC: | 21839-101 |
| Proprietary Name: | Multivitamin Bodyblock |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, and Oxybenzone |
| Active Ingredient(s): | 2.5; 9.4; 6.25; 3.75 mL/125mL; mL/125mL; mL/125mL; mL/125mL & nbsp; Avobenzone, Octinoxate, Octisalate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 21839-101 |
| Labeler Name: | Gordon Laboratories, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20051101 |
| Package NDC: | 21839-101-25 |
| Package Description: | 1 TUBE in 1 BOX (21839-101-25) > 125 mL in 1 TUBE |
| NDC Code | 21839-101-25 |
| Proprietary Name | Multivitamin Bodyblock |
| Package Description | 1 TUBE in 1 BOX (21839-101-25) > 125 mL in 1 TUBE |
| Product NDC | 21839-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20051101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Gordon Laboratories, Inc |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 2.5; 9.4; 6.25; 3.75 |
| Strength Unit | mL/125mL; mL/125mL; mL/125mL; mL/125mL |
| Pharmaceutical Classes |