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DDF Daily Protective Moisturizer
DDF Daily Protective Moisturizer - 37000-334-48 - (Avobenzone, Homosalate, Octisalate, and Octocrylene)
Drug Information of DDF Daily Protective Moisturizer
| Product NDC: | 37000-334 |
| Proprietary Name: | DDF Daily Protective Moisturizer |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Active Ingredient(s): | .03; .05; .05; .026 g/g; g/g; g/g; g/g & nbsp; Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DDF Daily Protective Moisturizer
| Product NDC: | 37000-334 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110901 |
Package Information of DDF Daily Protective Moisturizer
| Package NDC: | 37000-334-48 |
| Package Description: | 1 TUBE in 1 CARTON (37000-334-48) > 48 g in 1 TUBE |
NDC Information of DDF Daily Protective Moisturizer
| NDC Code | 37000-334-48 |
| Proprietary Name | DDF Daily Protective Moisturizer |
| Package Description | 1 TUBE in 1 CARTON (37000-334-48) > 48 g in 1 TUBE |
| Product NDC | 37000-334 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | .03; .05; .05; .026 |
| Strength Unit | g/g; g/g; g/g; g/g |
| Pharmaceutical Classes |
