Label: BABYFRESH PETROLEUM JELLY- petrolatum jelly

  • NDC Code(s): 61734-050-03, 61734-050-04, 61734-050-05, 61734-050-06
  • Packager: Delon Laboratories (1990) Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 24, 2023

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  • Active Ingredient



    White Petrolatum USP (99.7%)

  • 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 more 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 ingredient

    fragrance

  • Delon Baby Fresh Petroleum Jelly 13 oz (368 g)

    Delon Baby Fresh Petroleum Jelly 13oz

  • Eboline Baby Fresh Petroleum Jelly 13 oz (368 g)

    Eboline Baby Fresh Petroleum Jelly 13oz

  • INGREDIENTS AND APPEARANCE
    BABYFRESH PETROLEUM JELLY 
    petrolatum jelly
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61734-050
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM99.7 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    TALC (UNII: 7SEV7J4R1U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61734-050-03368 g in 1 JAR; Type 0: Not a Combination Product05/07/201005/31/2024
    2NDC:61734-050-04212 g in 1 JAR; Type 0: Not a Combination Product05/07/201007/31/2023
    3NDC:61734-050-0590 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/04/201412/04/2014
    4NDC:61734-050-06170 g in 1 JAR; Type 0: Not a Combination Product02/14/201911/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01605/07/201005/31/2024
    Labeler - Delon Laboratories (1990) Ltd (248364184)
    Establishment
    NameAddressID/FEIBusiness Operations
    Laboratoires Delon208896216label(61734-050) , pack(61734-050) , manufacture(61734-050)
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