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NDC 30142-0522-21 SUNSCREEN 30; 150; 50; 100 mg/mL; mg/mL; mg/mL; mg/mL Details
SUNSCREEN 30; 150; 50; 100 mg/mL; mg/mL; mg/mL; mg/mL
SUNSCREEN is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by The Kroger Co. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE.
Product Information
NDC | 30142-0522 |
---|---|
Product ID | 30142-522_c57c96e6-d721-4178-80d8-f076439acc08 |
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 |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Avobenzone, Homosalate, Octisalat, Octocrylene |
Product Type | HUMAN OTC DRUG |
Dosage Form | LOTION |
Route | TOPICAL |
Active Ingredient Strength | 30; 150; 50; 100 |
Active Ingredient Units | mg/mL; mg/mL; mg/mL; mg/mL |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
Labeler Name | The Kroger Co |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part352 |
Listing Certified Through | 2024-12-31 |
Package
NDC 30142-0522-21 (30142052221)
NDC Package Code | 30142-522-21 |
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Billing NDC | 30142052221 |
Package | 88 mL in 1 TUBE (30142-522-21) |
Marketing Start Date | 2021-11-30 |
NDC Exclude Flag | N |
Pricing Information | N/A |