Label: SHEA BUTTER PETROLEUM JELLY- petrolatum jelly jelly

  • NDC Code(s): 30400-501-01, 30400-501-02, 30400-501-03, 30400-501-04, view more
    30400-501-05, 30400-501-06, 30400-501-07, 30400-501-08
  • Packager: Jell Pharmaceuticals Pvt. Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 17, 2024

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  • Active Ingredient

    White Petrolatum USP (99.6%)

  • Purpose

    Skin Protectant

  • Uses

    temporarily protects minor: cuts, scrapes, burns; temporarily protects and helps relieve chapped or cracked skin and lips; helps protect from the drying effects of wind and cold weather

  • Warnings

    For external use only

  • When using this product

    do not get into eyes

  • Stop use and ask a doctor if

    condition worsens, symptoms last longer than 7 days or clear up and occur again within a few days

  • Do not use on

    deep or puncture wounds, animal bites, serious burns

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    apply as needed

  • Inactive ingredients

    butyrospermum parkii (shea butter), fragrance

  • Questions or comments?

    1-800-925-4733

  • Label

    Shea Butter Petroleum Jelly

  • INGREDIENTS AND APPEARANCE
    SHEA BUTTER PETROLEUM JELLY 
    petrolatum jelly jelly
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30400-501
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM99.6 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SHEA BUTTER (UNII: K49155WL9Y) 0.1 g  in 100 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30400-501-01368 g in 1 JAR; Type 0: Not a Combination Product10/11/2021
    2NDC:30400-501-0249 g in 1 JAR; Type 0: Not a Combination Product10/11/2021
    3NDC:30400-501-03100 g in 1 JAR; Type 0: Not a Combination Product10/11/2021
    4NDC:30400-501-04113 g in 1 JAR; Type 0: Not a Combination Product10/11/2021
    5NDC:30400-501-05170 g in 1 JAR; Type 0: Not a Combination Product10/11/2021
    6NDC:30400-501-06425 g in 1 JAR; Type 0: Not a Combination Product10/11/2021
    7NDC:30400-501-07226 g in 1 JAR; Type 0: Not a Combination Product10/11/2021
    8NDC:30400-501-08283 g in 1 JAR; Type 0: Not a Combination Product10/11/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01605/10/2021
    Labeler - Jell Pharmaceuticals Pvt. Ltd. (726025211)
    Registrant - Jell Pharmaceuticals Pvt. Ltd. (726025211)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jell Pharmaceuticals Pvt. Ltd.726025211manufacture(30400-501)
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