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NDC 46007-0203-21 SUNSCREEN MOISTURIZER 3; 7; 7.5; 5; 3; 6 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL Details
SUNSCREEN MOISTURIZER 3; 7; 7.5; 5; 3; 6 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
SUNSCREEN MOISTURIZER is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by Skin Authority LLC. The primary component is AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE.
Product Information
| NDC | 46007-0203 |
|---|---|
| Product ID | 46007-203_06fe49cf-6c88-81d9-e063-6294a90a6af2 |
| 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 | SUNSCREEN MOISTURIZER |
| Proprietary Name Suffix | SPF 30 |
| Non-Proprietary Name | AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LOTION |
| Route | TOPICAL |
| Active Ingredient Strength | 3; 7; 7.5; 5; 3; 6 |
| Active Ingredient Units | g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Labeler Name | Skin Authority LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M020 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 46007-0203-21 (46007020321)
| NDC Package Code | 46007-203-21 |
|---|---|
| Billing NDC | 46007020321 |
| Package | 20 mL in 1 TUBE (46007-203-21) |
| Marketing Start Date | 2012-04-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |