NDC | 58400-007-01, 58400-007-02 |
Set ID | 7bfa0e42-c909-40c3-9f7e-e0c2ca2ba16a |
Category | HUMAN OTC DRUG LABEL |
Packager | Pharmco Laboratories Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
- Directions
- Other Ingredients
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Skin Cancer/Skin Aging Alert & Sun Protection Measures
Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m.-2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
This product has been shown to help prevent sun burn, not skin cancer or early skin aging.
- Other Information
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 87 g Tube Label
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INGREDIENTS AND APPEARANCE
DAILY FACIAL MOISTURIZER SPF 35
octinoxate and avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58400-007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 40 mg in 1 g Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 25 mg in 1 g Inactive Ingredients Ingredient Name Strength Aloe (UNII: V5VD430YW9) Benzyl Alcohol (UNII: LKG8494WBH) Carthamus Tinctorius Seed Oleosomes (UNII: 9S60Q72309) Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ) C13-14 Isoparaffin (UNII: E4F12ROE70) Laureth-7 (UNII: Z95S6G8201) Methylisothiazolinone (UNII: 229D0E1QFA) Sodium Hydroxide (UNII: 55X04QC32I) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58400-007-01 87 g in 1 TUBE; Type 0: Not a Combination Product 06/01/2012 2 NDC:58400-007-02 3900 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part352 06/01/2012 Labeler - Pharmco Laboratories Inc. (096270814) Establishment Name Address ID/FEI Business Operations Pharmco Laboratories Inc. 096270814 MANUFACTURE(58400-007) , LABEL(58400-007) , PACK(58400-007) , ANALYSIS(58400-007)