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Mommy Tillia
Mommy Tillia - 10096-0238-1 - (ALCOHOL)
Drug Information of Mommy Tillia
| Product NDC: | 10096-0238 |
| Proprietary Name: | Mommy Tillia |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | 153.34 mL/237mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mommy Tillia
| Product NDC: | 10096-0238 |
| Labeler Name: | Avon Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101220 |
Package Information of Mommy Tillia
| Package NDC: | 10096-0238-1 |
| Package Description: | 237 mL in 1 BOTTLE, DISPENSING (10096-0238-1) |
NDC Information of Mommy Tillia
| NDC Code | 10096-0238-1 |
| Proprietary Name | Mommy Tillia |
| Package Description | 237 mL in 1 BOTTLE, DISPENSING (10096-0238-1) |
| Product NDC | 10096-0238 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20101220 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Avon Products, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | 153.34 |
| Strength Unit | mL/237mL |
| Pharmaceutical Classes |
