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NDC 70764-0205-52 CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING 6.9; 3; 4 g/100mL; g/100mL; g/100mL Details
CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING 6.9; 3; 4 g/100mL; g/100mL; g/100mL
CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING 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 | 70764-0205 |
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Product ID | 70764-205_05f609b5-8cfd-9b7b-e063-6394a90ad8ba |
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 INTENSIVE SKIN BRIGHTENING |
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 | 2024-12-31 |
Package
NDC 70764-0205-52 (70764020552)
NDC Package Code | 70764-205-52 |
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Billing NDC | 70764020552 |
Package | 1 TUBE in 1 BOX (70764-205-52) / 74 mL in 1 TUBE (70764-205-22) |
Marketing Start Date | 2018-09-11 |
NDC Exclude Flag | N |
Pricing Information | N/A |