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NDC 49035-0566-49 Sunscreen ULTRA Broad Spectrum 30; 150; 50; 70 mg/mL; mg/mL; mg/mL; mg/mL Details
Sunscreen ULTRA Broad Spectrum 30; 150; 50; 70 mg/mL; mg/mL; mg/mL; mg/mL
Sunscreen ULTRA Broad Spectrum is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by WAL-MART STORES INC.. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE.
Product Information
| NDC | 49035-0566 |
|---|---|
| Product ID | 49035-566_f114cece-5d87-360c-e053-2a95a90ab3cc |
| 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 ULTRA Broad Spectrum |
| Proprietary Name Suffix | Equate |
| Non-Proprietary Name | Avobenzone Homosalate Octisalate Octocrylene |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LOTION |
| Route | TOPICAL |
| Active Ingredient Strength | 30; 150; 50; 70 |
| Active Ingredient Units | mg/mL; mg/mL; mg/mL; mg/mL |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Labeler Name | WAL-MART STORES INC. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part352 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 49035-0566-49 (49035056649)
| NDC Package Code | 49035-566-49 |
|---|---|
| Billing NDC | 49035056649 |
| Package | 44.4 mL in 1 BOTTLE (49035-566-49) |
| Marketing Start Date | 2020-10-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |