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NDC 49967-0971-01 Kiehls Since 1851 Activated Sun Protector Broad Spectrum SPF 30 Sunscreen Water Resistant 80 MInutes 22.4; 80; 24; 44.8; 28.8 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details
Kiehls Since 1851 Activated Sun Protector Broad Spectrum SPF 30 Sunscreen Water Resistant 80 MInutes 22.4; 80; 24; 44.8; 28.8 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Kiehls Since 1851 Activated Sun Protector Broad Spectrum SPF 30 Sunscreen Water Resistant 80 MInutes is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by L'Oreal USA Products Inc. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE.
Product Information
| NDC | 49967-0971 |
|---|---|
| Product ID | 49967-971_cac3e9bc-baae-4979-b643-23992b3a0748 |
| 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 | Kiehls Since 1851 Activated Sun Protector Broad Spectrum SPF 30 Sunscreen Water Resistant 80 MInutes |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LOTION |
| Route | TOPICAL |
| Active Ingredient Strength | 22.4; 80; 24; 44.8; 28.8 |
| Active Ingredient Units | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Labeler Name | L'Oreal USA Products Inc |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M020 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 49967-0971-01 (49967097101)
| NDC Package Code | 49967-971-01 |
|---|---|
| Billing NDC | 49967097101 |
| Package | 150 mL in 1 TUBE (49967-971-01) |
| Marketing Start Date | 2015-02-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |