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NDC 30142-0687-38 Sunscreen 30; 150; 50; 60 mg/g; mg/g; mg/g; mg/g Details
Sunscreen 30; 150; 50; 60 mg/g; mg/g; mg/g; mg/g
Sunscreen is a TOPICAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by The Kroger Co. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE.
Product Information
NDC | 30142-0687 |
---|---|
Product ID | 30142-687_a60b693d-2248-4b2b-b77e-a53545e5a325 |
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, Octisalate, Oxybenzone |
Product Type | HUMAN OTC DRUG |
Dosage Form | SPRAY |
Route | TOPICAL |
Active Ingredient Strength | 30; 150; 50; 60 |
Active Ingredient Units | mg/g; mg/g; mg/g; mg/g |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
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 30142-0687-38 (30142068738)
NDC Package Code | 30142-687-38 |
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Billing NDC | 30142068738 |
Package | 283 g in 1 BOTTLE, SPRAY (30142-687-38) |
Marketing Start Date | 2017-08-07 |
NDC Exclude Flag | N |
Pricing Information | N/A |