Label: SNUGZ SPF 50 SUNSCREEN STICK- spf 50 sunstick stick
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Contains inactivated NDC Code(s)
NDC Code(s): 76309-500-01, 76309-500-55, 76309-500-66 - Packager: SnugZ/USA, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 12, 2019
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- SnugZ SPF 50 Sunscreen Stick
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INGREDIENTS AND APPEARANCE
SNUGZ SPF 50 SUNSCREEN STICK
spf 50 sunstick stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76309-500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 0.561 g in 18.7 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.187 g in 18.7 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 0.561 g in 18.7 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76309-500-01 4.67 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2018 2 NDC:76309-500-55 14.8 g in 1 APPLICATOR; Type 0: Not a Combination Product 01/01/2018 3 NDC:76309-500-66 18.7 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/01/2018 Labeler - SnugZ/USA, LLC (615959228) Establishment Name Address ID/FEI Business Operations SnugZ/USA, LLC 615959228 manufacture(76309-500)
