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Mentholatum Natural Ice
Mentholatum Natural Ice - 10742-8980-1 - (avobenzone, dimethicone, octinoxate, octisalate)
Drug Information of Mentholatum Natural Ice
| Product NDC: | 10742-8980 |
| Proprietary Name: | Mentholatum Natural Ice |
| Non Proprietary Name: | avobenzone, dimethicone, octinoxate, octisalate |
| Active Ingredient(s): | 30; 10; 75; 50 mg/g; mg/g; mg/g; mg/g & nbsp; avobenzone, dimethicone, octinoxate, octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mentholatum Natural Ice
| Product NDC: | 10742-8980 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20000329 |
Package Information of Mentholatum Natural Ice
| Package NDC: | 10742-8980-1 |
| Package Description: | 1 TUBE in 1 BLISTER PACK (10742-8980-1) > 4.5 g in 1 TUBE |
NDC Information of Mentholatum Natural Ice
| NDC Code | 10742-8980-1 |
| Proprietary Name | Mentholatum Natural Ice |
| Package Description | 1 TUBE in 1 BLISTER PACK (10742-8980-1) > 4.5 g in 1 TUBE |
| Product NDC | 10742-8980 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | avobenzone, dimethicone, octinoxate, octisalate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20000329 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | AVOBENZONE; DIMETHICONE; OCTINOXATE; OCTISALATE |
| Strength Number | 30; 10; 75; 50 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
