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NDC 70764-0203-52 CONTROL CORRECTIVE DAY 6.9; 3; 4 g/100mL; g/100mL; g/100mL Details
CONTROL CORRECTIVE DAY 6.9; 3; 4 g/100mL; g/100mL; g/100mL
CONTROL CORRECTIVE DAY is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by CONTROL CORRECTIVE SKINCARE INC. The primary component is OCTINOXATE; OCTISALATE; ZINC OXIDE.
Product Information
| NDC | 70764-0203 |
|---|---|
| Product ID | 70764-203_d4f165b0-1c74-2dbe-e053-2a95a90a2b11 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | CONTROL CORRECTIVE DAY |
| Proprietary Name Suffix | SPF-30 SUNSCREEN |
| Non-Proprietary Name | OCTINOXATE, OCTISALATE, ZINC OXIDE |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 6.9; 3; 4 |
| Active Ingredient Units | g/100mL; g/100mL; g/100mL |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Labeler Name | CONTROL CORRECTIVE SKINCARE INC |
| Pharmaceutical Class | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part352 |
| Listing Certified Through | 2023-12-31 |
Package
NDC 70764-0203-52 (70764020352)
| NDC Package Code | 70764-203-52 |
|---|---|
| Billing NDC | 70764020352 |
| Package | 1 BOTTLE in 1 BOX (70764-203-52) / 74 mL in 1 BOTTLE (70764-203-22) |
| Marketing Start Date | 2018-09-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |