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Avon Sun
Avon Sun - 10096-0296-1 - (Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone, Octocrylene)
Drug Information of Avon Sun
| Product NDC: | 10096-0296 |
| Proprietary Name: | Avon Sun |
| Non Proprietary Name: | Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone, Octocrylene |
| Active Ingredient(s): | 28.5; 80; 75; 47.5; 25.6; 47.5 mg/g; mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone, Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Avon Sun
| Product NDC: | 10096-0296 |
| Labeler Name: | Avon Products, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130326 |
Package Information of Avon Sun
| Package NDC: | 10096-0296-1 |
| Package Description: | 136.5 g in 1 BOTTLE, SPRAY (10096-0296-1) |
NDC Information of Avon Sun
| NDC Code | 10096-0296-1 |
| Proprietary Name | Avon Sun |
| Package Description | 136.5 g in 1 BOTTLE, SPRAY (10096-0296-1) |
| Product NDC | 10096-0296 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate, Octinoxate, Octisalate, Oxybenzone, Avobenzone, Octocrylene |
| Dosage Form Name | AEROSOL, SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20130326 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Avon Products, Inc |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 28.5; 80; 75; 47.5; 25.6; 47.5 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
